510(k) K951576

FS-34P2, FIBER SIGMOIDOSCOPE by Pentax Precision Instrument Corp. — Product Code FAM

K951576 is an FDA 510(k) premarket notification submitted by Pentax Precision Instrument Corp. for the device "FS-34P2, FIBER SIGMOIDOSCOPE". The FDA issued a decision of Substantially Equivalent on June 29, 1995. 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 29, 1995
Date Received
April 4, 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