(245 days)
Not Found
No
The description details a purely electromechanical system for oxygen generation and storage using physical processes (molecular sieve) and standard controls, with no mention of AI or ML.
Yes
The device is intended to generate, store, and dispense USP grade oxygen for supplemental oxygen use, which is a therapeutic purpose.
No
The device is an oxygen concentrator and storage system intended to generate, store, and deliver oxygen for supplemental use, not to diagnose a medical condition. While it has an "integral oxygen analyzer," this is for controlling oxygen purity within the device, not for patient diagnosis.
No
The device description explicitly states that the EDOCS is an "electromechanical device consisting primarily of a molecular sieve type oxygen concentrator, a compressor module(s), and one or more oxygen collection cylinders." It also describes the MOST as a "oxygen storage and distribution system consisting of lightweight, high-pressure, composite wound, brass lined cylinders and a distribution manifold." These are clearly hardware components, not software only.
Based on the provided information, no, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices intended to be used in vitro for the examination of specimens, including blood, tissue, and urine, from the human body to provide information for diagnostic, monitoring, or compatibility purposes.
- Device Function: The EDOCS and MOST devices are designed to generate, store, and deliver oxygen for supplemental oxygen use. This is a therapeutic function, providing a substance to the body, rather than analyzing a specimen from the body to gain diagnostic information.
- Intended Use: The intended use clearly states "to generate and deliver USP grade 93% +/- 3% oxygen for supplemental oxygen use" and "to store and dispense USP grade 93% (+7%/-3%) oxygen... for supplemental oxygen use." This aligns with a therapeutic purpose, not an in vitro diagnostic one.
- Device Description: The description details the process of separating nitrogen from air to produce oxygen and the storage and distribution of that oxygen. There is no mention of analyzing biological specimens.
- Lack of IVD Indicators: The document does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples (blood, urine, tissue, etc.)
- Providing diagnostic information
- Using reagents or assays
- Image processing of biological samples
- AI/ML for analyzing biological data
Therefore, the EDOCS and MOST devices are therapeutic devices used to provide oxygen, not in vitro diagnostic devices used to analyze biological specimens for diagnostic purposes.
N/A
Intended Use / Indications for Use
The Expeditionary Deployable Oxygen Concentration System (EDOCS-120B) is intended to generate and deliver USP grade 93% +/- 3% oxygen for supplemental oxygen use. This device is to be used only by trained personnel in disaster relief situations where bottled oxygen is not readily available.
The Mobile Oxygen Storage Tank (MOST) is intended to store and dispense USP grade 93% (+7%/-3%) oxygen at 50psig nominal pressure for supplemental oxygen use. This device is to be used only by trained personnel in disaster relief situations where bottled oxygen is not readily available.
Product codes (comma separated list FDA assigned to the subject device)
CAW
Device Description
Expeditionary Deployable Oxygen Concentration System (EDOCS): The Expeditionary Deployable Oxygen Concentration System (EDOCS) is a family of devices that draw in normal air and produce oxygen. The EDOCS separates nitrogen from the air, producing an output of concentrated oxygen at 93 percent by the molecular sieve process. The final product contains not less than 90 percent and not more than 96 percent oxygen, by volume. The remainder of the product consists mostly of argon and nitrogen.
EDOCS employs an integral oxygen analyzer to provide control of oxygen purity.
The EDOCS device is an electromechanical device consisting primarily of a molecular sieve type oxygen concentrator, a compressor module(s), and one or more oxygen collection cylinders. The oxygen concentrator operates by adsorbing water and nitrogen from filtered air. Depending on the unit size, the resulting gas has increased oxygen at flow rates from 30 to 500 liters per minute at a pressure of 50 - 100 psi nominal and is capable of high pressure cylinder filling.
Mobile Oxygen Storage Tank (MOST): The Mobile Oxygen Storage Tank (MOST) is a oxygen storage and distribution system consisting of lightweight, high-pressure, composite wound, brass lined cylinders and a distribution manifold secured within a rugged waterproof case. The MOST contains 10,000 liters of oxygen when filled to 2,250 psig (13,400 liters at 3,000 psig). The MOST has a maximum flow capability of 225 LPM, which is equivalent to 75 LPM per Oxygen Output fitting (3 fittings per MOST). These three oxygen output flows would typically be subdivided further by the customer's equipment.
The small footprint, relatively light weight and easy carrying of the MOST system make it optimal for emergency use and military deployments. Eight handles, two on each long side of the MOST and two on the top at each end are provided for ease of transportation. The MOST contains the Apparatus Kit, which includes the equipment required to distribute the oxygen to up to three patients concurrently. The exterior dimensions of the MOST are: a length of 37.25", a width of 27.18", and height of 15.44." The MOST weighs approximately 200 pounds when charged to 2,250 psig.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
trained personnel in disaster relief situations where bottled oxygen is not readily available.
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Expeditionary Deployable Oxygen Concentration System (EDOCS): Verification and validation testing activities were conducted to establish the performance and reliability characteristics of the EDOCS, to demonstrate performance as intended and substantial equivalency to predicate device. Testing involved the following areas:
- Purity I
- Flow Rate
- Electrical Safety
- Mechanical
- Controls
- Device Performance
Acceptance criteria were based on US Army specifications (USAMMA), and those established in voluntary standards.
In all instances the device met all required performance criteria and functioned as intended, meeting the acceptance criteria.
Mobile Oxygen Storage Tank (MOST): Verification and validation testing activities were conducted to establish the performance, reliability and safety characteristics of the MOST and to demonstrate performance as intended. Testing involved the following areas:
- Purity
- Flow Rate
- Mechanical
- Controls
- Device Performance
- Safety
Acceptance criteria were based on USAF specifications (AFMESA), DOT-CFFC, NASA and MIL-STD-810F.
In all instances the device met all required performance criteria and functioned as intended, meeting the acceptance criteria.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 868.5440 Portable oxygen generator.
(a)
Identification. A portable oxygen generator is a device that is intended to release oxygen for respiratory therapy by means of either a chemical reaction or physical means (e.g., a molecular sieve).(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/0 description: The image shows the logo for Pacific Consolidated Industries. The logo consists of a stylized triangle with the letters "PCI" embedded within it. To the right of the logo is the text "Pacific Consolidated Industries" in a bold, sans-serif font.
510(k) Summary
JAN 2 2 2007
Expeditionary Deployable Oxygen Concentration System (EDOCS) & Mobile Oxygen Storage Tank (MOST)
| Type of FDA Submission | Traditional 510(k) |
|---|---|
| Submitter Information | |
| Submitter's Name: | Pacific Consolidated Industries |
| Submitter's Address: | 12201 Magnolia Avenue |
| Riverside, California 92503-4820 | |
| Owner/Operator ID: | 9049531 |
| Contact Person: | Gary W. Clark |
| Submitter's Phone: | (951) 479-0872 (Phone) |
| (951) 479-0861 (Fax) | |
| Date of Preparation: | January 12, 2007 |
| Device Classification | |
| Classification Name: | Portable Oxygen Generator |
| Device Classification: | 868.5440 |
| Product Code: | CAW |
| Panel: | Anesthesiology and Respiratory Therapy Devices |
1
Image /page/1/Picture/0 description: The image shows the logo for Pacific Consolidated Industries. The logo consists of a stylized triangle with the letters "P", "C", and "I" incorporated into the design. To the right of the logo is the text "Pacific Consolidated Industries" in a bold, sans-serif font.
Expeditionary Deployable Oxygen Concentration System (EDOCS)
Predicate Legally Marketed Device Equivalence
Substantial equivalence is claimed to the legally marketed predicate device previously submitted under K020330 - Deployable Oxygen Concentration System (DOCS).
Safe Medical Devices Act (SMDA) Statement
The oxygen supplied by the oxygen concentrator is supplemental and is not considered to be life supporting or life sustaining. The failure of the device would not have serious health consequences to the user.
Intended Use of Device
The Expeditionary Deployable Oxygen Concentration System (EDOCS-120B) is intended to . generate and deliver USP grade 93% +/- 3% oxygen for supplemental oxygen use. This device is to be used only by trained personnel in disaster relief situations where bottled oxygen is not readily available.
Description of Device
The Expeditionary Deployable Oxygen Concentration System (EDOCS) is a family of devices that draw in normal air and produce oxygen. The EDOCS separates nitrogen from the air, producing an output of concentrated oxygen at 93 percent by the molecular sieve process. The final product contains not less than 90 percent and not more than 96 percent oxygen, by volume. The remainder of the product consists mostly of argon and nitrogen.
EDOCS employs an integral oxygen analyzer to provide control of oxygen purity.
The EDOCS device is an electromechanical device consisting primarily of a molecular sieve type oxygen concentrator, a compressor module(s), and one or more oxygen collection cylinders. The oxygen concentrator operates by adsorbing water and nitrogen from filtered air. Depending on the unit size, the resulting gas has increased oxygen at flow rates from 30 to 500 liters per minute at a pressure of 50 - 100 psi nominal and is capable of high pressure cylinder filling.
Device Labeling
The EDOCS is clearly labeled with the following:
- 93% ±3% Oxygen .
- Contraindications, for example, oil-rich or flammable atmosphere .
- Rx Only
2
Image /page/2/Picture/0 description: The image shows the logo for Pacific Consolidated Industries. The logo consists of a stylized triangle on the left, with the words "Pacific Consolidated Industries" to the right of the triangle. The triangle is made up of three horizontal lines, with the top line being the shortest and the bottom line being the longest.
Comparison of Technological Characteristics
The technological characteristics of these devices and their intended use to supply supplemental oxygen are the same as the predicate devices and raise no new questions of safety and effectiveness.
Special Controls/Conformance to Recognized Standards
The Expeditionary Deployable Oxygen Concentration System (EDOCS) conforms to the recognized standard USP 24-NF 19 (through Supplement Four, December 31, 2001) and employs an integral oxygen analyzer to provide control of oxygen purity in accordance with the standard.
The EDOCS has been tested under IEC 60601-1-2 and has passed the required Electromagnetic Compatibility tests.
A Risk Analysis, as described in ISO 14971, has been conducted on the EDOCS and all identified risks have been managed to the degree possible via design, engineering controls or labeling.
Summary of Performance Testing
Verification and validation testing activities were conducted to establish the performance and reliability characteristics of the EDOCS, to demonstrate performance as intended and substantial equivalency to predicate device. Testing involved the following areas:
- Purity I
- 피 Flow Rate
- Electrical Safety ■
- 트 Mechanical
- 해 Controls
- 피 Device Performance
Acceptance criteria were based on US Army specifications (USAMMA), and those established in voluntary standards.
In all instances the device met all required performance criteria and functioned as intended, meeting the acceptance criteria.
Conclusions
In summary, Pacific Consolidated Industries has demonstrated that the EDOCS meets its specifications, is safe and effective for its intended use, and is substantially equivalent to the currently marketed devices.
3
Image /page/3/Picture/0 description: The image shows the logo for Pacific Consolidated Industries. The logo consists of a stylized letter "A" on the left, followed by the company name "Pacific Consolidated Industries" in bold, sans-serif font. The letter "A" is formed by three horizontal lines stacked on top of each other, creating a triangular shape.
Mobile Oxygen Storage Tank (MOST)
Predicate Legally Marketed Device Equivalence
Substantial equivalence is claimed to the legally marketed predicate device previously submitted under K040738 - Mobile Oxygen Storage Tank (MOST).
Safe Medical Devices Act (SMDA) Statement
The oxygen supplied by the MOST is supplemental and is not considered to be life supporting or life sustaining. The failure of the device would not have serious health consequences to the user.
Description of Device
The Mobile Oxygen Storage Tank (MOST) is a oxygen storage and distribution system consisting of lightweight, high-pressure, composite wound, brass lined cylinders and a distribution manifold secured within a rugged waterproof case. The MOST contains 10,000 liters of oxygen when filled to 2,250 psig (13,400 liters at 3,000 psig). The MOST has a maximum flow capability of 225 LPM, which is equivalent to 75 LPM per Oxygen Output fitting (3 fittings per MOST). These three oxygen output flows would typically be subdivided further by the customer's equipment.
The small footprint, relatively light weight and easy carrying of the MOST system make it optimal for emergency use and military deployments. Eight handles, two on each long side of the MOST and two on the top at each end are provided for ease of transportation. The MOST contains the Apparatus Kit, which includes the equipment required to distribute the oxygen to up to three patients concurrently. The exterior dimensions of the MOST are: a length of 37.25", a width of 27.18", and height of 15.44." The MOST weighs approximately 200 pounds when charged to 2,250 psig.
Intended Use of Device
The Mobile Oxygen Storage Tank (MOST) is intended to store and dispense USP grade 93% (+7%/-3%) oxygen at 50 psig nominal pressure for supplemental oxygen use. This device is to be used only by trained personnel in disaster relief situations where bottled oxygen is not readily available.
Device Labeling
The MOST is clearly labeled with the following:
- 93% +7%1-3% Oxygen .
- Contraindications, for example, oil-rich or flammable atmosphere
- Rx Only
4
Image /page/4/Picture/0 description: The image shows the logo for Pacific Consolidated Industries. The logo consists of a stylized letter "A" on the left, followed by the company name in a sans-serif font. The letter "A" is formed by three horizontal lines connecting the two sides of the triangle.
Comparison of Technological Characteristics
There are no significant changes in the MOST unit in this submission from that of the original submission.
Special Controls/Conformance to Recognized Standards
The Mobile Oxygen Storage Tank (MOST) conforms to the DOT-CFFC standard.
A Risk Analysis, as described in ISO 14971, has been conducted on the MOST and all identified risks have been managed to the degree possible via design, engineering controls or labeling.
Summary of Performance Testing
Verification and validation testing activities were conducted to establish the performance, reliability and safety characteristics of the MOST and to demonstrate performance as intended. Testing involved the following areas:
- Purity
- Flow Rate
- Mechanical
- 트 Controls
- Device Performance
- Safety
Acceptance criteria were based on USAF specifications (AFMESA), DOT-CFFC, NASA and MIL-STD-810F.
In all instances the device met all required performance criteria and functioned as intended, meeting the acceptance criteria.
Conclusions
In summary, Pacific Consolidated Industries has demonstrated that the MOST meets its specifications, is safe and effective in providing a portable supply of USP oxygen to the intended markets, and is substantially equivalent to the currently marketed device.
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Image /page/5/Picture/1 description: The image shows the seal of the Department of Health & Human Services (HHS). The seal features a stylized eagle with its wings spread, clutching a staff with a snake wrapped around it. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES . USA" are arranged in a circular pattern around the eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
JAN 2 2 2007
Mr. Gary Clark Vice President-Regulatory Affairs/ Ouality Assurance Pacific Consolidated Industries, LLC 12201 Magnolia Avenue Riverside, California 92503-4820
Re: K061414
Trade/Device Name: Expeditionary Deployable Oxygen Concentration System (EDOCS-120B) Regulation Number: 868.5440 Regulation Name: Portable Oxygen Generator Regulatory Class: II Product Code: CAW Dated: January 12, 2007 Received: January 16, 2007
Dear Mr. Clark:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into cither class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
6
Page 2 - Mr. Clark
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Chiu Lin, Ph.D.
Director Division of Anesthesiology, General Hospital. Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
7
Statement of Indications for Use
Name: Expeditionary Deployable Oxygen Concentration System (EDOCS-120B)
The Expeditionary Deployable Oxygen Concentration System (EDOCS-120B) is intended to generate and deliver USP grade 93% +/- 3% oxygen for supplemental oxygen use. This device is to be used only by trained personnel in disaster relief situations where bottled oxygen is not readily available.
Name: Mobile Oxygen Storage Tank (MOST)
The Mobile Oxygen Storage Tank (MOST) is intended to store and dispense USP grade 93% (+7%/-3%) oxygen at 50psig nominal pressure for supplemental oxygen use. This device is to be used only by trained personnel in disaster relief situations where bottled oxygen is not readily available.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use X (Per 21 CFR 801.109)
Mell Zelen
Anesthesiology, General Hospital
Pain Control, Cranial Devices
Number: K061414