The following data is part of a premarket notification filed by Star Instrument Co. with the FDA for Crouch Corneal Protector.
| Device ID | K833256 |
| 510k Number | K833256 |
| Device Name: | CROUCH CORNEAL PROTECTOR |
| Classification | Shield, Eye, Ophthalmic (including Sunlamp Protective Eyewear And Post-mydriatic Eyewear) |
| Applicant | STAR INSTRUMENT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HOY |
| CFR Regulation Number | 886.4750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-20 |
| Decision Date | 1984-02-08 |