510(k) K100803
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