Latex Penrose Drain Tubing
FDA 510(k) K821700 · Abco Dealers, Inc.
510(k) numberK821700
Submission
- Device name
- Latex Penrose Drain Tubing
- Applicant
- Abco Dealers, Inc.
Mchenry, IL, US - Received
- June 8, 1982
- Decision date
- June 16, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- GAX – Tourniquet, Nonpneumatic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.5900
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code GAX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K931198 | UniquetGAX · Traditional | Icat Systems | 09/01/1993SE |
| K881398 | TourniquetGAX · Traditional | Barretta Products, Research and Development, Inc. | 04/29/1988SE |
| K881176 | Sterile Esmarch BandageGAX · Traditional | Spectrum/Hydro-Med Products, Inc. | 04/11/1988SE |
| K875092 | Degania Silicone TourniquetGAX · Traditional | Degania Silicone , Ltd. | 01/07/1988SE |
| K873928 | Universal TourniquetGAX · Traditional | Dryden Corp. | 10/23/1987SE |
| K872003 | KinderwrapGAX · Traditional | The Kinder Co. | 06/23/1987SE |
| K864897 | Dale Venipuncture Tourniquet, Product No. 1335GAX · Traditional | Dale Medical Products, Inc. | 01/12/1987SE |
| K853472 | Finger TourniquetteGAX · Traditional | Joseph B. Marogil | 10/10/1985SE |
| K853537 | Velcro TourniquetGAX · Traditional | Cp Medical | 09/12/1985SE |
| K852277 | Catapress TourniguetGAX · Traditional | Boehringer Ingelheim Pharmaceuticals, Inc. | 06/27/1985SE |
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| 510(k) | Device | Decision |
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| K880892 | Blood Collecting Needle and HoldersFMI · Traditional | 04/21/1988SE |
| K880894 | Allergist SyringesFMF · Traditional | 03/31/1988SE |
| K872875 | Stretch Gauze BandagesNAD · Traditional | 09/04/1987SE |
| K872874 | Microscope Cover GlassesKES · Traditional | 08/10/1987SE |
| K872797 | Non-Skid Shoe CoversFXP · Traditional | 08/04/1987SE |
| K871465 | Thermometer SheathsFLL · Traditional | 05/11/1987SE |
| K862726 | Disposable Shoe Covers and Nurses CapsFXP · Traditional | 08/01/1986SE |
| K862111 | Armboards, Reusable and Disposable · Traditional | 07/08/1986SE |
Questions and answers
When was Latex Penrose Drain Tubing cleared by the FDA?
Latex Penrose Drain Tubing (K821700) received a 510(k) decision of Substantially Equivalent on June 16, 1982, 8 days after the submission was received.
What is the product code of K821700?
The FDA product code is GAX – Tourniquet, Nonpneumatic, a Class I (low risk) device regulated under 21 CFR 878.5900.