FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

EPPENDORF DILUTER

K Number: K844798 · Decision Jan 7, 1985
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
6
Review Days
27

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Basic Information

Device Name
EPPENDORF DILUTER
K Number
K844798
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2750
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Medical Technomics, Ltd.
Date Received
December 11, 1984
Decision Date
January 7, 1985
Product Code
JQW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JQW Station, Pipetting And Diluting, For Clinical Use

Similar 510(k) Clearances

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Other Clearances by Medical Technomics, Ltd.

K Number Device Name
K843608 CAPILLARY BLOOD COLLECTION TUBE
K843607 LABOPETTOR
K843361 MINICAPS
K843606 PRECISION DISPENSER
K843362 RINGCAPS