The following data is part of a premarket notification filed by Bioclinical Laboratory Services, Inc. with the FDA for Chondroitin Sulfate Corneal Storage Medium.
Device ID | K870251 |
510k Number | K870251 |
Device Name: | CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM |
Classification | Media, Corneal Storage |
Applicant | BIOCLINICAL LABORATORY SERVICES, INC. 9310 HUNTING VALLEY RD. Clarence, NY 14031 |
Contact | Fike, Phd |
Correspondent | Fike, Phd BIOCLINICAL LABORATORY SERVICES, INC. 9310 HUNTING VALLEY RD. Clarence, NY 14031 |
Product Code | LYX |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-01-21 |
Decision Date | 1987-04-06 |