VESSEL-CLUDE
Clamp, Surgical, General & Plastic Surgery
MED GENERAL
The following data is part of a premarket notification filed by Med General with the FDA for Vessel-clude.
Pre-market Notification Details
| Device ID | K771701 |
| 510k Number | K771701 |
| Device Name: | VESSEL-CLUDE |
| Classification | Clamp, Surgical, General & Plastic Surgery |
| Applicant | MED GENERAL 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GDJ |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-09-08 |
| Decision Date | 1977-12-13 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10886333222435 | K771701 | 000 |
| 10886333222428 | K771701 | 000 |
| 10886333222411 | K771701 | 000 |
| 10886333222404 | K771701 | 000 |
| 10886333222398 | K771701 | 000 |
| 10886333222381 | K771701 | 000 |
Trademark Results [VESSEL-CLUDE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VESSEL-CLUDE 73151383 1107139 Dead/Expired |
MED GENERAL, INC. 1977-12-08 |
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