510(k) K961567

ES-3840, VIDEO SIGMOIDOSCOPE by Pentax Precision Instrument Corp. — Product Code FAM

K961567 is an FDA 510(k) premarket notification submitted by Pentax Precision Instrument Corp. for the device "ES-3840, VIDEO SIGMOIDOSCOPE". The FDA issued a decision of Substantially Equivalent on June 24, 1996. The device falls under product code FAM (Sigmoidoscope And Accessories, Flexible/Rigid), a Class II device regulated under 21 CFR 876.1500. Pentax Precision Instrument Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 24, 1996
Date Received
April 23, 1996
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