510(k) K892387
K892387 is an FDA 510(k) premarket notification submitted by Gelman Sciences, Inc. for the device "MODIFIED GELMAN ARTERIAL FILTER". The FDA issued a decision of Substantially Equivalent on June 22, 1989. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Gelman Sciences, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 22, 1989
- Date Received
- April 14, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Filter, Blood, Cardiopulmonary Bypass, Arterial Line
- Device Class
- Class II
- Regulation Number
- 870.4260
- Review Panel
- CV
- Submission Type