Conphar Oxygen Catheter-Sterile
FDA 510(k) K791273 · Conphar, Inc.
510(k) numberK791273
Submission
- Device name
- Conphar Oxygen Catheter-Sterile
- Applicant
- Conphar, Inc.
Mchenry, IL, US - Received
- July 6, 1979
- Decision date
- July 24, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BZB – Catheter, Nasal, Oxygen
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.5350
- Specialty
- Anesthesiology
Other 510(k)s with product code BZB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K896731 | Oxygen CathetersBZB · Traditional | Unoplast A/S | 03/30/1990SE |
| K843466 | Pharma-Plast Oxygen CatheterBZB · Traditional | Zimmar Consulting , Ltd. | 11/19/1984SE |
| K833351 | Demand Oxygen ControllerBZB · Traditional | Healthdyne, Inc. | 03/19/1984SE |
| K830984 | Oxygen CathetersBZB · Traditional | Medovations, Inc. | 05/18/1983SE |
| K820370 | Nasal Oxygen CatheterBZB · Traditional | American Pharmaseal Div. Ahsc | 04/16/1982SE |
| K800506 | Oxygen CatheterBZB · Traditional | Medi-Craft , Ltd. | 03/25/1980SE |
| K790057 | Catheter, OxygenBZB · Traditional | Medline Industries, Inc. | 02/05/1979SE |
More from Medline Industries, Inc.
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| K821825 | Conphar Silicone Feeding TubeKNT · Traditional | 08/10/1982SE |
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| K821295 | Olsen Hegar Needle HoldersGDF · Traditional | 06/03/1982SE |
| K821289 | Mayo-Hegar Needle HolderGDF · Traditional | 06/03/1982SE |
| K821298 | Backhaus Clamp, 3 1/2HTD · Traditional | 05/28/1982SE |
| K821294 | Tonsil Scissors Straight 5 1/2EGN · Traditional | 05/28/1982SE |
| K821293 | Backhaus Clamp, 5 1/4HTD · Traditional | 05/28/1982SE |
| K821292 | Tonsil Scissors 7EGN · Traditional | 05/28/1982SE |
| K821290 | Littauer Scissors 5 1/2HNF · Traditional | 05/28/1982SE |
| K821286 | Iris Scissors Straight 4 1/2HNF · Traditional | 05/28/1982SE |
Questions and answers
When was Conphar Oxygen Catheter-Sterile cleared by the FDA?
Conphar Oxygen Catheter-Sterile (K791273) received a 510(k) decision of Substantially Equivalent on July 24, 1979, 18 days after the submission was received.
What is the product code of K791273?
The FDA product code is BZB – Catheter, Nasal, Oxygen, a Class I (low risk) device regulated under 21 CFR 868.5350.