510(k) K940651
K940651 is an FDA 510(k) premarket notification submitted by 3M Health Care, Sarns for the device "SARNS ULTRASONIC AIR SENSOR". The FDA issued a decision of Substantially Equivalent on May 24, 1994. The device falls under product code KRL (Detector, Bubble, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4205. 3M Health Care, Sarns has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 24, 1994
- Date Received
- February 15, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Detector, Bubble, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4205
- Review Panel
- CV
- Submission Type