510(k) K950429

VIDEO SIGMOIDOSCOPE by Welch Allyn, Inc. — Product Code FAM

K950429 is an FDA 510(k) premarket notification submitted by Welch Allyn, Inc. for the device "VIDEO SIGMOIDOSCOPE". The FDA issued a decision of Substantially Equivalent on August 1, 1995. The device falls under product code FAM (Sigmoidoscope And Accessories, Flexible/Rigid), a Class II device regulated under 21 CFR 876.1500. Welch Allyn, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 1995
Date Received
February 2, 1995
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