510(k) K030726
K030726 is an FDA 510(k) premarket notification submitted by Gish Biomedical, Inc. for the device "GISH CAPVRF44 HARDSHELL VENOUS RESERVOIR WITH GBS COATING". The FDA issued a decision of Substantially Equivalent on May 30, 2003. The device falls under product code DTN (Reservoir, Blood, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4400. Gish Biomedical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 30, 2003
- Date Received
- March 7, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Reservoir, Blood, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4400
- Review Panel
- CV
- Submission Type