510(k) K962506

[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)] by Gynecare Innovation Center — Product Code FJL

K962506 is an FDA 510(k) premarket notification submitted by Gynecare Innovation Center for the device "[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)]". The FDA issued a decision of Substantially Equivalent on September 16, 1996. The device falls under product code FJL (Resectoscope), a Class II device regulated under 21 CFR 876.1500. Gynecare Innovation Center has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 1996
Date Received
June 27, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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