The following data is part of a premarket notification filed by Ocular Instruments, Inc. with the FDA for Hoskins Nylon Suture Laser Lens.
Device ID | K862728 |
510k Number | K862728 |
Device Name: | HOSKINS NYLON SUTURE LASER LENS |
Classification | Lens, Contact, Polymethylmethacrylate, Diagnostic |
Applicant | OCULAR INSTRUMENTS, INC. 12100 NORTHUP WAY SUITE D Bellevue, WA 98005 |
Contact | Tamsin J Erickson |
Correspondent | Tamsin J Erickson OCULAR INSTRUMENTS, INC. 12100 NORTHUP WAY SUITE D Bellevue, WA 98005 |
Product Code | HJK |
CFR Regulation Number | 886.1385 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-18 |
Decision Date | 1986-08-21 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00630238106511 | K862728 | 000 |
00630238100007 | K862728 | 000 |
00630238007054 | K862728 | 000 |