The following data is part of a premarket notification filed by Civco Medical Instruments Co., Inc. with the FDA for Civco Scan Drape.
Device ID | K844472 |
510k Number | K844472 |
Device Name: | CIVCO SCAN DRAPE |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | CIVCO MEDICAL INSTRUMENTS CO., INC. 418 B AVE. Kalona, IA 52247 |
Contact | Victor J Wedel |
Correspondent | Victor J Wedel CIVCO MEDICAL INSTRUMENTS CO., INC. 418 B AVE. Kalona, IA 52247 |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-11-19 |
Decision Date | 1985-01-23 |