The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Cordis Biopsy Forceps.
| Device ID | K810849 |
| 510k Number | K810849 |
| Device Name: | CORDIS BIOPSY FORCEPS |
| Classification | Device, Biopsy, Endomyocardial |
| Applicant | CORDIS CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DWZ |
| CFR Regulation Number | 870.4075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-03-30 |
| Decision Date | 1981-04-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20705032056110 | K810849 | 000 |
| 20705032056103 | K810849 | 000 |
| 20705032056097 | K810849 | 000 |
| 20705032056127 | K810849 | 000 |