510(k) K862774
K862774 is an FDA 510(k) premarket notification submitted by American Bioproducts Co. for the device "ASSERACHROM PF4 KIT". The FDA issued a decision of Substantially Equivalent on September 4, 1986. The device falls under product code LCO (Platelet Factor 4 Radioimmunoassay), a Class II device regulated under 21 CFR 864.7695. American Bioproducts Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 4, 1986
- Date Received
- July 22, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Platelet Factor 4 Radioimmunoassay
- Device Class
- Class II
- Regulation Number
- 864.7695
- Review Panel
- HE
- Submission Type