510(k) K930496

GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS by Birtcher Medical Systems, Inc. — Product Code GCI

K930496 is an FDA 510(k) premarket notification submitted by Birtcher Medical Systems, Inc. for the device "GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS". The FDA issued a decision of Substantially Equivalent on April 20, 1993. The device falls under product code GCI (Laryngoscope, Endoscope), a Class II device regulated under 21 CFR 876.1500. Birtcher Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 1993
Date Received
February 1, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Laryngoscope, Endoscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
SU
Submission Type