510(k) K031432
K031432 is an FDA 510(k) premarket notification submitted by Hk Surgical, Inc. for the device "KLEIN SURGICAL INFILTRATION PUMP, MODEL KIP-II". The FDA issued a decision of Substantially Equivalent on August 7, 2003. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. Hk Surgical, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 7, 2003
- Date Received
- May 6, 2003
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Infusion
- Device Class
- Class II
- Regulation Number
- 880.5725
- Review Panel
- HO
- Submission Type