CLAMPEASE FA
Clamp, Vascular
FREUND MEDICAL PRODUCTS
The following data is part of a premarket notification filed by Freund Medical Products with the FDA for Clampease Fa.
Pre-market Notification Details
| Device ID | K863427 |
| 510k Number | K863427 |
| Device Name: | CLAMPEASE FA |
| Classification | Clamp, Vascular |
| Applicant | FREUND MEDICAL PRODUCTS 401 EAST FIFTH ST. Dayton, OH 45402 |
| Contact | Robert K Garner |
| Correspondent | Robert K Garner FREUND MEDICAL PRODUCTS 401 EAST FIFTH ST. Dayton, OH 45402 |
| Product Code | DXC |
| CFR Regulation Number | 870.4450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-09-04 |
| Decision Date | 1986-11-20 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20815614021044 | K863427 | 000 |
| 30815614020358 | K863427 | 000 |
Trademark Results [CLAMPEASE FA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CLAMPEASE FA 73619780 1441118 Dead/Cancelled |
FREUND MEDICAL PRODUCTS, INC. 1986-09-15 |
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