The following data is part of a premarket notification filed by The Brewer Co. with the FDA for Brewer Company Teddy Crib Model 71900-a, B, 71910-a, B.
| Device ID | K950051 |
| 510k Number | K950051 |
| Device Name: | BREWER COMPANY TEDDY CRIB MODEL 71900-A, B, 71910-A, B |
| Classification | Bed, Pediatric Open Hospital |
| Applicant | THE BREWER CO. 13901 MAIN ST. P.O. BOX 159 Menomonee Falls, WI 53051 |
| Contact | Joseph H Hannes |
| Correspondent | Joseph H Hannes THE BREWER CO. 13901 MAIN ST. P.O. BOX 159 Menomonee Falls, WI 53051 |
| Product Code | FMS |
| CFR Regulation Number | 880.5140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-01-06 |
| Decision Date | 1995-02-10 |