The following data is part of a premarket notification filed by Life-tech Intl., Inc. with the FDA for Urethralpressure Profile Catheter.
Device ID | K915484 |
510k Number | K915484 |
Device Name: | URETHRALPRESSURE PROFILE CATHETER |
Classification | Cystometric Gas (carbon-dioxide) On Hydraulic Device |
Applicant | LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
Contact | Alfred C Coats |
Correspondent | Alfred C Coats LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
Product Code | FAP |
CFR Regulation Number | 876.1620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-12-06 |
Decision Date | 1992-02-24 |