(289 days)
The Deployable Oxygen Concentration System (DOCS) Family of devices generates and delivers USP grade 93% ± 3% oxygen. The oxygen supplied by these units is for supplemental not considered to be life supporting or life sustaining.
DOCS Family devices may be used to fill high pressure oxygen cylinders for use in locations remote to the DOCS unit or for ambulatory patient use.
These devices are to be used only by trained personnel in disaster relief, crisis response or humanitarian relief situations where bottled or bulk oxygen is not readily available, as hospital backup systems, in local emergencies where disaster has rendered the primary oxygen supply unusable, or by trained military personnel in peacetime or wartime support of Armed Forces.
The Deployable Oxygen Concentration System (DOCS) is a family of electromechanical devices that use a molecular sieve to adsorb nitrogen, water and carbon dioxide from filtered air, producing an output of high purity oxygen (93 ± 3 %) via the Vacuum Swing Adsorption process. The remainder of the gas product consists mostly of argon and nitrogen.
Depending on the unit size, the resulting high purity oxygen can be delivered at flow rates ranging from 66 to 500 liters per minute at a pressure of 50 - 100 psig under standard conditions.
Selected models may be configured with one or two integral high pressure compressors or an accessory high pressure compressor may be added to some models. These high pressure units are capable of filling oxygen cylinders to 2,250 or 3,000 psig.
The provided text describes the acceptance criteria and a summary of performance testing for the Deployable Oxygen Concentration System (DOCS) family.
1. Table of Acceptance Criteria and Reported Device Performance
While the document doesn't provide a precise numerical table of acceptance criteria for each specific characteristic, it broadly states the following:
| Acceptance Criteria Category | Reported Device Performance |
|---|---|
| Purity | Generates and delivers USP grade 93% ± 3% oxygen. Monitored and controlled by an integral oxygen analyzer. |
| Flow Rate | Ranges from 66 to 500 liters per minute at a pressure of 50 - 100 psig under standard conditions (depending on unit size). |
| Electrical Safety | Met all required performance criteria per IEC 60601-1-1 ("Safety requirements for medical electrical systems"). |
| Mechanical Operation | Met all required performance criteria. |
| Hardware and Software Controls | Met all required performance criteria. |
| Environmental Conditions | Met all required performance criteria. |
| Overall Functionality | Functioned as intended, meeting acceptance criteria. |
| Equivalence | Substantially equivalent to predicate devices, raising no new questions of safety and effectiveness. |
| Standards Conformance | Conforms to USP 30-NF 25. |
| Electromagnetic Compatibility | Passed required tests per IEC 60601-1-2. |
2. Sample Size Used for the Test Set and Data Provenance
The document does not specify the sample size used for the test set or the data provenance (e.g., country of origin, retrospective/prospective). It only mentions "Testing was conducted to establish the performance and reliability characteristics of the DOCS family."
3. Number of Experts Used to Establish Ground Truth for the Test Set and Their Qualifications
This information is not provided in the document. The testing appears to be focused on technical performance and adherence to standards rather than expert-derived ground truth.
4. Adjudication Method for the Test Set
This information is not provided in the document.
5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study
A multi-reader multi-case (MRMC) comparative effectiveness study was not mentioned. The testing described is focused on the device's technical performance and compliance with relevant standards.
6. Standalone (Algorithm Only Without Human-in-the-Loop Performance) Study
The testing described is inherently a standalone performance evaluation of the device itself (the Deployable Oxygen Concentration System). There is no "algorithm" in the sense of AI being evaluated, but rather the electromechanical system. The "Summary of Performance Testing" refers to the device's ability to meet specified criteria and function as intended without human intervention in its core oxygen generation process.
7. Type of Ground Truth Used
The "ground truth" for the performance testing appears to be based on:
- Established Technical Specifications: Purity (USP grade 93% ± 3% oxygen), Flow Rate (66 to 500 L/min), and Pressure (50-100 psig).
- Recognized Standards: USP 30-NF 25, IEC 60601-1-1 (Electrical Safety), and IEC 60601-1-2 (Electromagnetic Compatibility).
- Intended Use Parameters: Functionality under specified environmental conditions and mechanical operation.
8. Sample Size for the Training Set
This product is an electromechanical device, not an AI algorithm, so there is no concept of a training set in the context of machine learning.
9. How the Ground Truth for the Training Set Was Established
As this is not an AI algorithm, this question is not applicable.
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K100959 polintl.com
510(k) Summary
Deployable Oxygen Concentration System (DOCS)
JAN 2 1 2011
1
| Type of FDA Submission | Traditional 510(k) |
|---|---|
| Submitter Information | |
| Submitter's Name: | Pacific Consolidated Industries |
| Submitter's Address: | 12201 Magnolia AvenueRiverside, 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: | April 5, 2010 |
| Device Classification | |
| Classification Name: | Portable Oxygen Generator |
| Device Classification: | 868.5440 |
| Product Code: | CAW |
| Panel: | Anesthesiology and Respiratory Therapy Devices |
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Delalatle Com
Image /page/1/Picture/1 description: The image shows the logo for PCI, which includes a triangular shape on the left and the letters "PCI" in bold font on the right. Below the logo, the text "advancing air separation technology" is written in a smaller font. The logo is black and white and appears to be a company logo.
Deployable Oxygen Concentration System (DOCS) Family
Predicate Legally Marketed Device Equivalence
Substantial equivalence is claimed to the legally marketed predicate devices previously submitted under K020330 - Deplovable Oxygen Concentration System (DOCS) and K061414 - Expeditionary Deployable Oxygen Concentration System (EDOCS) & Mobile Oxygen Storage Tank (MOST).
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 Deployable Oxygen Concentration System (DOCS) family of devices generates and delivers USP grade 93% ± 3% oxygen. The oxygen supplied by these units is for supplemental use and is not considered to be life supporting or life sustaining.
DOCS family devices may be used to fill high pressure oxygen cylinders for use in locations remote to the DOCS unit or for ambulatory patient use.
These devices are to be used only by trained personnel in disaster relief, crisis response or humanitarian relief situations where bottled or bulk oxygen is not readly available, as hospital backup systems, in focal emergencies where disaster has rendered the primary oxygen supply unusable, or by trained military personnel in peacetime or wartime support of Armed Forces.
Description of Device
The Deployable Oxygen Concentration System (DOCS) is a family of electromechanical devices that use a molecular sieve to adsorb nitrogen, water and carbon dioxide from filtered air, producing an output of high purity oxygen (93 ± 3 %) via the Vacuum Swing Adsorption process. The remainder of the gas product consists mostly of argon and nitrogen.
Depending on the unit size, the resulting high purity oxygen can be delivered at flow rates ranging from 66 to 500 liters per minute at a pressure of 50 - 100 psig under standard conditions.
Selected models may be configured with one or two integral high pressure compressors or an accessory high pressure compressor may be added to some models. These high pressure units are capable of filling oxygen cylinders to 2,250 or 3,000 psig.
Device Labeling
Each member of the DOCS family is clearly labeled with the following:
- 93% ±3% Oxygen .
- · Not for use in oil-rich or flammable atmosphere
- Rx Only
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.
| 12201 Magnolia Avenue, Riverside, CA 92503 |
|---|
| -------------------------------------------- |
| phone | 951.479.0860 |
|---|---|
| fax | 951.479.0861 |
| info@pci-intl.com |
2
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Image /page/2/Picture/0 description: The image shows the logo for PCI, which appears to be a company that specializes in air generation technology. The logo consists of a black triangle with a white curved line running through it, followed by the letters "PCI" in bold black font. Below the logo, the words "advancing air generation technology" are written in a smaller font.
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Special Controls/Conformance to Recognized Standards
The Deployable Oxygen Concentration System (DOCS) family conforms to the recognized standard USP 30-NF 25 and employs an integral oxygen analyzer to monitor and control oxygen purity in accordance with the standard.
The DOCS has been tested under IEC 60601-1-1 and has passed the required "Safety requirements for medical electrical systems" tests.
The DOCS has been tested under IEC 60601-1-2 and has passed the required Electromagnetic Compatibility tests.
Summary of Performance Testing
Testing was conducted to establish the performance and reliability characteristics of the DOCS family, to demonstrate performance as intended and substantial equivalency to predicate devices. Testing involved the following areas:
- Purity
- Flow Rate
- . Electrical Safety
- Mechanical Operation
- 트 Hardware and Software Controls
- l Environmental Conditions
In all instances the devices met all required performance criteria and functioned as intended, meeting the acceptance criteria.
Conclusions
In summary, Pacific Consolidated Industries has demonstrated that the DOCS family members meet their specifications, are safe and effective for their intended use, and are substantially equivalent to the currently marketed devices.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Mr. Gary Clark Pacific Consolidated Industries, LLC 12201 Magnolia Avenue Riverside, California 92503
JAN 2 1 2011
Re: K100957
Trade/Device Name: Deployable Oxygen System (DOCS) Family Regulation Number: 21 CFR 868.5440 Regulation Name: Portable Oxygen Generator Regulatory Class: II Product Code: CAW Dated: January 7, 2011 Received: January 11, 2011
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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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 Eederal Register.
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Page 2- Mr. Clark
Enclosure
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); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to
http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
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) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
for
Anthony D. Watson, B.S.,M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
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Indications for Use
510(k) Number (if known): 长100957
Device Name: Deployable Oxygen System (DOCS) Family
Indications For Use:
The Deployable Oxygen Concentration System (DOCS) Family of devices generates and delivers
USP grade 93% ± 3% oxygen. The oxygen supplied by these units is for supplemental not considered to be life supporting or life sustaining.
DOCS Family devices may be used to fill high pressure oxygen cylinders for use in locations remote to the DOCS unit or for ambulatory patient use.
These devices are to be used only by trained personnel in disaster relief, crisis response or humanitarian relief situations where bottled or bulk oxygen is not readily available, as hospital backup systems, in local emergencies where disaster has rendered the primary oxygen supply unusable, or by trained military personnel in peacetime or wartime support of Armed Forces,
Prescription Use _ × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Schultz
(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices
Page 1 of 1
510(k) Number: K2100957
§ 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).