(225 days)
Not Found
No
The summary describes a mechanical safety mechanism for an IV catheter and does not mention any AI or ML components or functions.
No
The device is an IV catheter used for administering fluids, sampling blood, and monitoring blood pressure. While it is used in therapeutic settings, its primary function is as an access device, not as a device that delivers therapy itself.
No
The device is described as an IV catheter used for sampling blood, monitoring blood pressure, or administering fluids, and it has a safety mechanism for needle sticks. None of these functions are diagnostic; they are interventional or for monitoring.
No
The device description clearly outlines physical components such as a stainless steel needle, Teflon catheter tube, hub, and a safety locking mechanism with a rubber band, indicating it is a hardware device.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is used for sampling blood, monitoring blood pressure, or administering fluids intravenously. These are procedures performed on the patient, not tests performed on samples taken from the patient to diagnose or monitor a condition.
- Device Description: The description details the physical components of an IV catheter, which is a device used for accessing the vascular system. It does not describe any components or functions related to analyzing biological samples.
- Lack of IVD Characteristics: The provided information does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples (blood, urine, tissue, etc.)
- Detecting or measuring specific substances in samples
- Providing diagnostic or monitoring information based on sample analysis
- Reagents or assays
The ComCaSet-P Safety IV Catheter is a medical device used for direct patient care involving vascular access.
N/A
Intended Use / Indications for Use
The ComCaSet-P Safety IV Catheter is indicated to sample blood, monitor blood pressure, or administer fluids intravenously. The ComCaSet-P Safety IV Catheter may be used for any patient population with consideration given to adequacy of the vascular anatomy appropriateness for the solution being administered and duration of the therapy. The ComCaSet-P Safety IV Catheter provides a shielding mechanism intended to reduce the incidence of accidental needle sticks. When the catheter hub and needle assembly components are withdrawn, the shielding mechanism is activated and the needle retracts into the shielding tube.
Product codes
FOZ
Device Description
The ComCaSet-P Safety IV Catheter consists of several parts common to most IV catheters: stainless steel needle, Teflon catheter tube with hub and the catheter body. In addition, the ComCaSet-P Safety IV Catheter has a safety locking mechanism which enables the needle and the flash chamber to retract into a safety barrel.
Disconnecting the needle assembly and catheter hub from the catheter releases the latex-free elastic rubber band and allows the needle and flash chamber to retract quickly into the safety barrel.
The product is available in seven gauges identified also by specific colors as follows:
Size: 14G, Color: Orange, Catheter I.D. mm: 1.7, Catheter O.D. mm: 2.1, Catheter Length(mm): 45, Water Flow Rate (ml./min.): 270
Size: 16G, Color: Grey, Catheter I.D. mm: 1.3, Catheter O.D. mm: 1.7, Catheter Length(mm): 45, Water Flow Rate (ml./min.): 180
Size: 17G, Color: White, Catheter I.D. mm: 1.1, Catheter O.D. mm: 1.5, Catheter Length(mm): 45, Water Flow Rate (ml./min.): 125
Size: 18G, Color: Green, Catheter I.D. mm: 0.9, Catheter O.D. mm: 1.3, Catheter Length(mm): 45, Water Flow Rate (ml./min.): 80
Size: 20G, Color: Pink, Catheter I.D. mm: 0.8, Catheter O.D. mm: 1.1, Catheter Length(mm): 32, Water Flow Rate (ml./min.): 54
Size: 22G, Color: Blue, Catheter I.D. mm: 0.6, Catheter O.D. mm: 0.9, Catheter Length(mm): 25, Water Flow Rate (ml./min.): 33
Size: 24G, Color: Yellow, Catheter I.D. mm: 0.5, Catheter O.D. mm: 0.7, Catheter Length(mm): 19, Water Flow Rate (ml./min.): 20
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
any patient population
Intended User / Care Setting
Not Found
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)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 880.5200 Intravascular catheter.
(a)
Identification. An intravascular catheter is a device that consists of a slender tube and any necessary connecting fittings and that is inserted into the patient's vascular system for short term use (less than 30 days) to sample blood, monitor blood pressure, or administer fluids intravenously. The device may be constructed of metal, rubber, plastic, or a combination of these materials.(b)
Classification. Class II (performance standards).
0
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Pitango Medical Ltd.
510(k) Summary:
ComCaSet-P Safety IV Catheter
AUG 1 6 2007
Company Name:
Pitango Medical Ltd. Ltd.
Contact Person: Ben Levin Managing Director Telephone: +972-3-613-0480 +972-3-613-0481 Fax: E-mail: belevin@pitangomedical.com
Authorized US Agent:
George J. Hattub, RAC & CQE Senior Staff Consultant MedicSense Inc. 291 Hillside Avenue Somerset, Massachusetts 02726
Phone: (508) 479-6116 (508) 677-1418 Fax: E-Mail: george@medicsense.com
Date prepared: December 27, 2006
Trade Name: ComCaSet-P Safety IV Catheter.
Classification name: Intravascular catheter
Class: II
Panel identification: General Hospital Devices
Product code: FOZ
Regulation number: 880.5200
Predicate Device: ComCaSet Safety IV Catheter, Pitango Medical Ltd, Ramat Gan, Israel, cleared under 510(k) no. 062108.
1
Pitango Medical Ltd.
Device description:
The ComCaSet-P Safety IV Catheter consists of several parts common to most IV catheters: stainless steel needle, Teflon catheter tube with hub and the catheter body. In addition, the ComCaSet-P Safety IV Catheter has a safety locking mechanism which enables the needle and the flash chamber to retract into a safety barrel
Disconnecting the needle assembly and catheter hub from the catheter releases the latex-free elastic rubber band and allows the needle and flash chamber to retract quickly into the safety barrel.
The product is available in seven gauges identified also by specific colors as follows:
| Size | Color | Catheter | | Catheter
Length(mm) | Water
Flow Rate
(ml./min.) |
|------|--------|------------|------------|------------------------|----------------------------------|
| | | I.D.
mm | O.D.
mm | | |
| 14G | Orange | 1.7 | 2.1 | 45 | 270 |
| 16G | Grey | 1.3 | 1.7 | 45 | 180 |
| 17G | White | 1.1 | 1.5 | 45 | 125 |
| 18G | Green | 0.9 | 1.3 | 45 | 80 |
| 20G | Pink | 0.8 | 1.1 | 32 | 54 |
| 22G | Blue | 0.6 | 0.9 | 25 | 33 |
| 24G | Yellow | 0.5 | 0.7 | 19 | 20 |
Indications for Use:
The ComCaSet-P Safety IV Catheter is indicated to sample blood, monitor blood pressure, or administer fluids intravenously. The ComCaSet-P Safety IV Catheter may be used for any patient population with consideration given to adequacy of the vascular anatomy appropriateness for the solution being administered and duration of the therapy. The ComCaSet-P Safety IV Catheter provides a shielding mechanism intended to reduce the incidence of accidental needle sticks. When the catheter hub and needle assembly components are withdrawn, the shielding mechanism is activated and the needle retracts into the shielding tube.
2
Pitango Medical Ltd.
Substantial Equivalence:
The ComCaSet Safety-P IV Catheter has the same intended use and the same principle of operation as the ComCaSet Safety IV Catheter cleared under 510(k) no. K062108. The main technological difference between ComCaSet-P Safety IV Catheter and the predicate devices is the release element of the needle retraction element, which at the ComCaSet-P Safety IV Catheter is activated by the separation of the catheter hub and needle assembly from the catheter.
Conclusion:
The evaluation of the ComCaSet-P Safety IV Catheter does not raise any additional concerns regarding safety and effectiveness and may therefore be considered substantially equivalent to the predicate device.
3
Image /page/3/Picture/1 description: The image shows the seal of the Department of Health & Human Services (HHS) of the United States. The seal features the department's name encircling a stylized image of an eagle. The eagle is depicted with three lines forming its body and wings, suggesting movement or flight.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Mr. Ben Levin Managing Director Pitango Medical Limited 3A Jabotinski Street, 28th Floor Diamond House-Doron Levy Ramat Gan, Israel 52520
AUG 16 2007
Re: K070020
Trade/Device Name: ComCaSet-P Safety IV Catheter Regulation Number: 880.5200 Regulation Name: Intravascular Catheter Regulatory Class: II Product Code: FOZ Dated: July 31, 2007 Received: August 6, 2007
Dear Mr. Levin:
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 either 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.
4
Page 2 - Mr. Levin
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 vour 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) 276-0115. 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.
Clus
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
5
Korodo
Indications for Use
510(k) Number (if known): _ KO 70020
Device Name: ComCaSet-P Safety IV Catheter
Indications for Use:
The ComCaSet-P Safety IV Catheter is indicated to sample blood, monitor blood pressure, or administer fluids intravenously. The ComCaSet-P Safety IV Catheter may be used for any patient population with consideration given to adequacy of the vascular anatomy appropriateness for the solution being administered and duration of the therapy. The ComCaSet-P Safety IV Catheter provides a shielding mechanism intended to reduce the incidence of accidental needle sticks. When the catheter hub and needle assembly components are withdrawn, the shielding mechanism is activated and the needle retracts into the shielding tube.
Prescription Use V (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Qhuls
mon Sign-Off) rsion of Anesthesiology, General Hospital Inrection Control, Dental Devices
umber. K070020
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