510(k) K890580
K890580 is an FDA 510(k) premarket notification submitted by North American Instrument Corp. for the device "LIPID STOPCOCK". The FDA issued a decision of Substantially Equivalent on April 19, 1989. The device falls under product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4290. North American Instrument Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 19, 1989
- Date Received
- February 6, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4290
- Review Panel
- CV
- Submission Type