510(k) K820790

FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3 by American Optical Corp. — Product Code FAM

K820790 is an FDA 510(k) premarket notification submitted by American Optical Corp. for the device "FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3". The FDA issued a decision of Substantially Equivalent on April 1, 1982. The device falls under product code FAM (Sigmoidoscope And Accessories, Flexible/Rigid), a Class II device regulated under 21 CFR 876.1500. American Optical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 1982
Date Received
March 23, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sigmoidoscope And Accessories, Flexible/Rigid
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

to examine and perform procedures within the sigmoid (descending) colon