The following data is part of a premarket notification filed by American Medical Systems, Inc. with the FDA for Entrac(tm) Urethral Measuring Catheter.
Device ID | K914905 |
510k Number | K914905 |
Device Name: | ENTRAC(TM) URETHRAL MEASURING CATHETER |
Classification | Catheter, Urethral |
Applicant | AMERICAN MEDICAL SYSTEMS, INC. 11001 BREN RD. EAST Minnetonka, MN 55343 |
Contact | Susan Tesmer |
Correspondent | Susan Tesmer AMERICAN MEDICAL SYSTEMS, INC. 11001 BREN RD. EAST Minnetonka, MN 55343 |
Product Code | GBM |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-11-01 |
Decision Date | 1992-03-20 |