The following data is part of a premarket notification filed by Bt Medical Co., Inc. with the FDA for Pneumatic Compression Device.
Device ID | K930885 |
510k Number | K930885 |
Device Name: | PNEUMATIC COMPRESSION DEVICE |
Classification | System, X-ray, Fluoroscopic, Image-intensified |
Applicant | BT MEDICAL CO., INC. SECOND AND DEPOT Bridgeport, PA 19405 |
Contact | Buckley Thompson |
Correspondent | Buckley Thompson BT MEDICAL CO., INC. SECOND AND DEPOT Bridgeport, PA 19405 |
Product Code | JAA |
CFR Regulation Number | 892.1650 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-02-18 |
Decision Date | 1993-07-13 |