Vessel-Clude
FDA 510(k) K771701 · Med General
510(k) numberK771701
Submission
- Device name
- Vessel-Clude
- Applicant
- Med General
Mchenry, IL, US - Received
- September 8, 1977
- Decision date
- December 13, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- GDJ – Clamp, Surgical, General & Plastic Surgery
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code GDJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K153358 | Standard ClampGDJ · Traditional | Standard Bariatrics | 05/02/2016SE |
| K930315 | Thoracic Clamps: Sarot, Kantowitz and LawrenceGDJ · Traditional | Thomasville Medical Assoc. | 02/04/1994SE |
| K924223 | Mar-Med Liver StrapGDJ · Traditional | Mar-Med Co. | 03/18/1993SE |
| K922659 | General Surgery Clamp and Needle HolderGDJ · Traditional | Miltex Instrument Co. | 07/21/1992SE |
| K914913 | Grice Foot Pedal Control/Reddick Irri/Aspir SystGDJ · Traditional | Ideal Medical, Inc. | 12/31/1991SE |
| K900956 | GS-7100 Cholangiogram Clamp, 5MMGDJ · Traditional | Solos Endoscopy, Inc. | 04/18/1990SE |
| K901107 | Modified Auto Suture Purstring Disp. AutomaticGDJ · Traditional | United States Surgical, A Division of Tyco Healthc | 04/09/1990SE |
| K895726 | Vessel OccluderGDJ · Traditional | Applied Medical Technologies | 10/24/1989SE |
| K895591 | Silicone Instrument ShodsGDJ · Traditional | Key Surgical, Inc. | 10/20/1989SE |
| K882169 | Surgical Duct Clamp (Vine)GDJ · Traditional | Henley Intl. | 06/17/1988SE |
More from Henley Intl.
| 510(k) | Device | Decision |
|---|---|---|
| K791097 | Ceptortrode with Ceptor HesiveGXY · Traditional | 08/03/1979SE |
| K791098 | Single-Use Mini-BulldogDXC · Traditional | 06/22/1979SE |
| K790763 | Maxi-Vac TMGCY · Traditional | 04/23/1979SE |
| K790269 | Ceptor HesiveGXY · Traditional | 02/26/1979SE |
| K782006 | Medgeneral Single-Use BulldogGDJ · Traditional | 12/15/1978SE |
| K781239 | Myo-StimIPF · Traditional | 11/03/1978SE |
| K780632 | MaxiceptorISB · Traditional | 08/14/1978SE |
| K780698 | Stimulators, Nerve, ElectricalGZJ · Traditional | 05/12/1978SE |
| K780117 | CardiometerDRT · Traditional | 02/03/1978SE |
| K771702 | Vessel-StabilizerKDC · Traditional | 12/13/1977SE |
Questions and answers
When was Vessel-Clude cleared by the FDA?
Vessel-Clude (K771701) received a 510(k) decision of Substantially Equivalent on December 13, 1977, 96 days after the submission was received.
What is the product code of K771701?
The FDA product code is GDJ – Clamp, Surgical, General & Plastic Surgery, a Class I (low risk) device regulated under 21 CFR 878.4800.