510(k) K100803

OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1 by Keymed, Inc. — Product Code FEQ

K100803 is an FDA 510(k) premarket notification submitted by Keymed, Inc. for the device "OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1". The FDA issued a decision of Substantially Equivalent on April 22, 2010. The device falls under product code FEQ (Pump, Air, Non-Manual, For Endoscope), a Class II device regulated under 21 CFR 876.1500. Keymed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 22, 2010
Date Received
March 22, 2010
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Air, Non-Manual, For Endoscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type