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

DILUTER, LSA 290 PIPETTER

K Number: K781883 · Decision Dec 4, 1978
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
92
Review Days
27

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Basic Information

Device Name
DILUTER, LSA 290 PIPETTER
K Number
K781883
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2750
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Kallestad Laboratories, Inc.
Date Received
November 7, 1978
Decision Date
December 4, 1978
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

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