510(k) K915484

URETHRALPRESSURE PROFILE CATHETER by Life-Tech Intl., Inc. — Product Code FAP

K915484 is an FDA 510(k) premarket notification submitted by Life-Tech Intl., Inc. for the device "URETHRALPRESSURE PROFILE CATHETER". The FDA issued a decision of Substantially Equivalent on February 24, 1992. The device falls under product code FAP (Cystometric Gas (Carbon-Dioxide) On Hydraulic Device), a Class II device regulated under 21 CFR 876.1620. Life-Tech Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1992
Date Received
December 6, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cystometric Gas (Carbon-Dioxide) On Hydraulic Device
Device Class
Class II
Regulation Number
876.1620
Review Panel
GU
Submission Type