The following data is part of a premarket notification filed by Bradstreet Clinical Research Assoc., Inc. with the FDA for Ryder Contact Lens Case Model 10670.
| Device ID | K951182 |
| 510k Number | K951182 |
| Device Name: | RYDER CONTACT LENS CASE MODEL 10670 |
| Classification | Case, Contact Lens |
| Applicant | BRADSTREET CLINICAL RESEARCH ASSOC., INC. 1588 ROUTE 130 NORTH SUITE C-2 North Brunswick, NJ 08902 |
| Contact | Patricia W Bradstreet |
| Correspondent | Patricia W Bradstreet BRADSTREET CLINICAL RESEARCH ASSOC., INC. 1588 ROUTE 130 NORTH SUITE C-2 North Brunswick, NJ 08902 |
| Product Code | LRX |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-16 |
| Decision Date | 1995-05-16 |