The following data is part of a premarket notification filed by Civco Medical Instruments Co., Inc. with the FDA for Verza Guidance System.
Device ID | K160806 |
510k Number | K160806 |
Device Name: | Verza Guidance System |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | CIVCO MEDICAL INSTRUMENTS CO., INC. 102 FIRST ST. SOUTH Kalona, IA 52247 |
Contact | Amanda Stahle |
Correspondent | Amanda Stahle CIVCO MEDICAL INSTRUMENTS CO., INC. 102 FIRST ST. SOUTH Kalona, IA 52247 |
Product Code | ITX |
CFR Regulation Number | 892.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-24 |
Decision Date | 2016-08-05 |
Summary: | summary |