The following data is part of a premarket notification filed by Alcon Laboratories with the FDA for Needles And Sutures, Silk & Nylon.
| Device ID | K760158 |
| 510k Number | K760158 |
| Device Name: | NEEDLES AND SUTURES, SILK & NYLON |
| Classification | Suture, Nonabsorbable, Silk |
| Applicant | ALCON LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GAP |
| CFR Regulation Number | 878.5030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-07-02 |
| Decision Date | 1976-08-19 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10380656987014 | K760158 | 000 |
| 10380651935010 | K760158 | 000 |
| 10380651934013 | K760158 | 000 |
| 10380651924014 | K760158 | 000 |
| 10380651876016 | K760158 | 000 |
| 10380651875019 | K760158 | 000 |
| 10380651860015 | K760158 | 000 |
| 10380651849010 | K760158 | 000 |
| 10380651848013 | K760158 | 000 |
| 10380651847016 | K760158 | 000 |
| 10380651846019 | K760158 | 000 |
| 10380651936017 | K760158 | 000 |
| 10380651956015 | K760158 | 000 |
| 10380656986017 | K760158 | 000 |
| 10380653072010 | K760158 | 000 |
| 10380653054016 | K760158 | 000 |
| 10380653052012 | K760158 | 000 |
| 10380652177013 | K760158 | 000 |
| 10380652053010 | K760158 | 000 |
| 10380652038017 | K760158 | 000 |
| 00380651987012 | K760158 | 000 |
| 10380651986012 | K760158 | 000 |
| 10380651963013 | K760158 | 000 |
| 10380651845012 | K760158 | 000 |