The following data is part of a premarket notification filed by Surgin Surgical Instrumentation, Inc. with the FDA for Opthalmic Wipe.
| Device ID | K942897 |
| 510k Number | K942897 |
| Device Name: | OPTHALMIC WIPE |
| Classification | Frame, Spectacle |
| Applicant | SURGIN SURGICAL INSTRUMENTATION, INC. 14762 BENTLEY CIRCLE Tustin, CA 92680 |
| Contact | Don W Haar |
| Correspondent | Don W Haar SURGIN SURGICAL INSTRUMENTATION, INC. 14762 BENTLEY CIRCLE Tustin, CA 92680 |
| Product Code | HQZ |
| CFR Regulation Number | 886.5842 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-20 |
| Decision Date | 1994-08-05 |