FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HEMOGLOBIN

K Number: K883683 · Decision Oct 6, 1988
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
36
Review Days
38

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Basic Information

Device Name
HEMOGLOBIN
K Number
K883683
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7500
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Tech-Co, Inc.
Date Received
August 29, 1988
Decision Date
October 6, 1988
Product Code
GJZ
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GJZ Cyanomethemoglobin Reagent And Standard Solution

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Other Clearances by Tech-Co, Inc.

K Number Device Name
K921968 IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST
K923376 VISUAL HCG PREGNANCY TEST
K920766 T4 EIA BEAD ASSAY
K920716 DIRECT PREGNANCY TEST
K902574 POTASSIUM REAGENT SET
K901561 IRON/TOTAL IRON BINDING CAPACITY
K883387 ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)
K883386 CHLORIDE
K881172 BILIRUBIN (DIRECT)
K881173 ASPARTATE AMINOTRANSFERASE (COLORIMETRIC METHOD)
Search all 36 clearances from Tech-Co, Inc. →