510(k) K821005
K821005 is an FDA 510(k) premarket notification submitted by Bio/Data Corp. for the device "PLATELET AGGREGATION PROFILER #PAP-4". The FDA issued a decision of Substantially Equivalent on June 1, 1982. The device falls under product code JBX (Aggregrometer, Platelet), a Class II device regulated under 21 CFR 864.6675. Bio/Data Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 1, 1982
- Date Received
- April 12, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Aggregrometer, Platelet
- Device Class
- Class II
- Regulation Number
- 864.6675
- Review Panel
- HE
- Submission Type