510(k) K911163

IMAGYN MEDICAL VIDEOSCOPY SYST W/IRRIG PUMP/ACCESS by Imagyn Medical, Inc. — Product Code FWF

K911163 is an FDA 510(k) premarket notification submitted by Imagyn Medical, Inc. for the device "IMAGYN MEDICAL VIDEOSCOPY SYST W/IRRIG PUMP/ACCESS". The FDA issued a decision of Substantially Equivalent on June 3, 1991. The device falls under product code FWF (Camera, Television, Endoscopic, Without Audio), a Class I device regulated under 21 CFR 878.4160. Imagyn Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 1991
Date Received
March 15, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Camera, Television, Endoscopic, Without Audio
Device Class
Class I
Regulation Number
878.4160
Review Panel
SU
Submission Type