510(k) K931954

THORACOSCOPE/LAPAROSCOPE by Surgical Technologies, Inc. — Product Code GCM

K931954 is an FDA 510(k) premarket notification submitted by Surgical Technologies, Inc. for the device "THORACOSCOPE/LAPAROSCOPE". The FDA issued a decision of Substantially Equivalent on November 2, 1993. The device falls under product code GCM (Endoscope, Rigid), a Class II device regulated under 21 CFR 876.1500. Surgical Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 2, 1993
Date Received
April 20, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscope, Rigid
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type