The following data is part of a premarket notification filed by Dmv Contact Lens Co. with the FDA for Dmv Angler.
| Device ID | K830496 |
| 510k Number | K830496 |
| Device Name: | DMV ANGLER |
| Classification | Inserter/remover Contact Lens |
| Applicant | DMV CONTACT LENS CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KYE |
| CFR Regulation Number | 886.5420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-16 |
| Decision Date | 1983-03-09 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00080875985916 | K830496 | 000 |
| 00080875971100 | K830496 | 000 |
| 00080875974231 | K830496 | 000 |
| 00080875974248 | K830496 | 000 |
| 00080875975016 | K830496 | 000 |
| 00080875975160 | K830496 | 000 |
| 00080875975290 | K830496 | 000 |
| 00080875975863 | K830496 | 000 |
| 00080875975955 | K830496 | 000 |
| 00080875983110 | K830496 | 000 |
| 00080875971094 | K830496 | 000 |