510(k) K791041
K791041 is an FDA 510(k) premarket notification submitted by Geometric Data, Div. Smithkline Corp. for the device "HEMATRAK ABNORMAL RECOGNITION". The FDA issued a decision of Substantially Equivalent on September 4, 1979. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Geometric Data, Div. Smithkline Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 4, 1979
- Date Received
- June 5, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Counter, Differential Cell
- Device Class
- Class II
- Regulation Number
- 864.5220
- Review Panel
- HE
- Submission Type