The following data is part of a premarket notification filed by Medical Device Inspection Co., Inc. with the FDA for Labor Delivery Tray.
Device ID | K912054 |
510k Number | K912054 |
Device Name: | LABOR DELIVERY TRAY |
Classification | Clamp, Umbilical |
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 | HFW |
CFR Regulation Number | 884.4530 [🔎] |
Decision | Substantially Equivalent - Kit (SESK) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-05-09 |
Decision Date | 1992-01-21 |