510(k) K771764
K771764 is an FDA 510(k) premarket notification submitted by 3M Health Care, Sarns for the device "CORONARY PRESSURE PERFUSION PUMP". The FDA issued a decision of Substantially Equivalent on September 30, 1977. The device falls under product code DXS (Gauge, Pressure, Coronary, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4310. 3M Health Care, Sarns has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 30, 1977
- Date Received
- September 19, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gauge, Pressure, Coronary, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4310
- Review Panel
- CV
- Submission Type