ACCU-PATH
Forceps, Biopsy, Non-electric
COX MEDICAL ENT., INC.
The following data is part of a premarket notification filed by Cox Medical Ent., Inc. with the FDA for Accu-path.
Pre-market Notification Details
| Device ID | K935250 |
| 510k Number | K935250 |
| Device Name: | ACCU-PATH |
| Classification | Forceps, Biopsy, Non-electric |
| Applicant | COX MEDICAL ENT., INC. 2186 EASTMAN AVE. SUITE 110 Ventura, CA 93003 |
| Contact | Lanita Cox |
| Correspondent | Lanita Cox COX MEDICAL ENT., INC. 2186 EASTMAN AVE. SUITE 110 Ventura, CA 93003 |
| Product Code | FCL |
| CFR Regulation Number | 876.1075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-01 |
| Decision Date | 1994-01-21 |
Trademark Results [ACCU-PATH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ACCU-PATH 75339772 not registered Dead/Abandoned |
ACCU-MED SERVICES, INC. 1997-08-12 |
 ACCU-PATH 74072504 not registered Dead/Abandoned |
PHELAN, JAMES C. 1990-06-25 |
 ACCU-PATH 73634465 1445028 Dead/Cancelled |
PFIZER HOSPITAL PRODUCTS GROUP, INC. 1986-12-09 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.