The following data is part of a premarket notification filed by Medical Device Inspection Co., Inc. with the FDA for C-section Tray.
| Device ID | K912075 |
| 510k Number | K912075 |
| Device Name: | C-SECTION TRAY |
| Classification | Instrument, Manual, Specialized Obstetric-gynecologic |
| Applicant | MEDICAL DEVICE INSPECTION CO., INC. 55 NORTHERN BLVD. SUITE 301 Great Neck, NY 11021 |
| Contact | Alan P.schwartz |
| Correspondent | Alan P.schwartz MEDICAL DEVICE INSPECTION CO., INC. 55 NORTHERN BLVD. SUITE 301 Great Neck, NY 11021 |
| Product Code | KNA |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent - Kit (SESK) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-05-10 |
| Decision Date | 1992-04-07 |