The following data is part of a premarket notification filed by Med-tron Products, Inc. with the FDA for Scanning Cot.
Device ID | K903901 |
510k Number | K903901 |
Device Name: | SCANNING COT |
Classification | Bed, Scanning, Nuclear |
Applicant | MED-TRON PRODUCTS, INC. P.O. BOX 866 Miller Place, NY 11764 |
Contact | Katherine Maguill |
Correspondent | Katherine Maguill MED-TRON PRODUCTS, INC. P.O. BOX 866 Miller Place, NY 11764 |
Product Code | IYZ |
CFR Regulation Number | 892.1350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-23 |
Decision Date | 1990-09-21 |