510(k) K904797

SURGITEK GRADUATED CYSTOSCOPE (MODEL GC-16) by Surgitek — Product Code FBO

K904797 is an FDA 510(k) premarket notification submitted by Surgitek for the device "SURGITEK GRADUATED CYSTOSCOPE (MODEL GC-16)". The FDA issued a decision of Substantially Equivalent on March 5, 1991. The device falls under product code FBO (Cystourethroscope), a Class II device regulated under 21 CFR 876.1500. Surgitek has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1991
Date Received
October 23, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cystourethroscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type