510(k) K850094
K850094 is an FDA 510(k) premarket notification submitted by Hematology Marketing Assoc. for the device "LASER-GLOBIN POWDER". The FDA issued a decision of Substantially Equivalent on March 29, 1985. The device falls under product code GKR (System, Hemoglobin, Automated), a Class II device regulated under 21 CFR 864.5620. Hematology Marketing Assoc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 29, 1985
- Date Received
- January 11, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Hemoglobin, Automated
- Device Class
- Class II
- Regulation Number
- 864.5620
- Review Panel
- HE
- Submission Type