The following data is part of a premarket notification filed by Lacrimedics, Inc. with the FDA for Herrick Ultimate Punctum Plug.
| Device ID | K963708 |
| 510k Number | K963708 |
| Device Name: | HERRICK ULTIMATE PUNCTUM PLUG |
| Classification | Plug, Punctum |
| Applicant | LACRIMEDICS, INC. 190 NORTH ARROWHEAD AVE., SUITE B Rialto, CA 92376 |
| Contact | Robert S Herrick |
| Correspondent | Robert S Herrick LACRIMEDICS, INC. 190 NORTH ARROWHEAD AVE., SUITE B Rialto, CA 92376 |
| Product Code | LZU |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-09-16 |
| Decision Date | 1997-04-14 |
| Summary: | summary |