The following data is part of a premarket notification filed by Ocular Instruments, Inc. with the FDA for Mainster High Magnification Laser Lens.
| Device ID | K912366 |
| 510k Number | K912366 |
| Device Name: | MAINSTER HIGH MAGNIFICATION LASER LENS |
| Classification | Lens, Contact, Polymethylmethacrylate, Diagnostic |
| Applicant | OCULAR INSTRUMENTS, INC. 2255 116TH AVE., N.E. Bellevue, WA 98004 -3039 |
| Contact | Tamsin J Erickson |
| Correspondent | Tamsin J Erickson OCULAR INSTRUMENTS, INC. 2255 116TH AVE., N.E. Bellevue, WA 98004 -3039 |
| Product Code | HJK |
| CFR Regulation Number | 886.1385 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-05-29 |
| Decision Date | 1991-06-25 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00630238031622 | K912366 | 000 |
| 00630238006996 | K912366 | 000 |