The following data is part of a premarket notification filed by Britt Corp., Inc. with the FDA for Britt Krypton Lasers 150k & 152k.
| Device ID | K813492 |
| 510k Number | K813492 |
| Device Name: | BRITT KRYPTON LASERS 150K & 152K |
| Classification | Laser, Ophthalmic |
| Applicant | BRITT CORP., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HQF |
| CFR Regulation Number | 886.4390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-11 |
| Decision Date | 1982-01-22 |