The following data is part of a premarket notification filed by Civco Medical Instruments Co., Inc. with the FDA for Disposable Transrectal/transvaginal/endocavity Ultrasound Needle Instrument Guide.
Device ID | K970514 |
510k Number | K970514 |
Device Name: | DISPOSABLE TRANSRECTAL/TRANSVAGINAL/ENDOCAVITY ULTRASOUND NEEDLE INSTRUMENT GUIDE |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | CIVCO MEDICAL INSTRUMENTS CO., INC. 102 1ST ST. SOUTH Kalona, IA 52247 |
Contact | J. William Jones |
Correspondent | J. William Jones CIVCO MEDICAL INSTRUMENTS CO., INC. 102 1ST 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 | 1997-02-11 |
Decision Date | 1997-06-20 |
Summary: | summary |