The following data is part of a premarket notification filed by Connecticut Bioinstruments, Inc. with the FDA for Weinstein Corneal Mircoaesthesiometer.
| Device ID | K920271 |
| 510k Number | K920271 |
| Device Name: | WEINSTEIN CORNEAL MIRCOAESTHESIOMETER |
| Classification | Esthesiometer, Ocular |
| Applicant | CONNECTICUT BIOINSTRUMENTS, INC. 5 B OAK LN. Danbury, CT 06811 |
| Contact | Curt Weinstein |
| Correspondent | Curt Weinstein CONNECTICUT BIOINSTRUMENTS, INC. 5 B OAK LN. Danbury, CT 06811 |
| Product Code | HJC |
| CFR Regulation Number | 886.1040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-22 |
| Decision Date | 1992-04-21 |