510(k) K844798
K844798 is an FDA 510(k) premarket notification submitted by Medical Technomics, Ltd. for the device "EPPENDORF DILUTER". The FDA issued a decision of Substantially Equivalent on January 7, 1985. The device falls under product code JQW (Station, Pipetting And Diluting, For Clinical Use), a Class I device regulated under 21 CFR 862.2750. Medical Technomics, Ltd. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 7, 1985
- Date Received
- December 11, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Station, Pipetting And Diluting, For Clinical Use
- Device Class
- Class I
- Regulation Number
- 862.2750
- Review Panel
- CH
- Submission Type