The following data is part of a premarket notification filed by G.w.b. Intl., Ltd. with the FDA for Ophta Sil (r), Punctal Plugs And Inserters.
Device ID | K911108 |
510k Number | K911108 |
Device Name: | OPHTA SIL (R), PUNCTAL PLUGS AND INSERTERS |
Classification | Plug, Punctum |
Applicant | G.W.B. INTL., LTD. P.O. BOX 801 Sudbury, MA 01776 |
Contact | George W Bohsack |
Correspondent | George W Bohsack G.W.B. INTL., LTD. P.O. BOX 801 Sudbury, MA 01776 |
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 | 1991-03-04 |
Decision Date | 1991-05-13 |