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

SERUM UIBC-PTF-600 METHOD

K Number: K831202 · Decision May 25, 1983
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
45
Applicant Total
73
Review Days
42

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Basic Information

Device Name
SERUM UIBC-PTF-600 METHOD
K Number
K831202
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1415
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Monitor Corp.
Date Received
April 13, 1983
Decision Date
May 25, 1983
Product Code
JMO
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
JMO Ferrozine (Colorimetric) Iron Binding Capacity

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JMO), ordered by most recent decision date.

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Other Clearances by American Monitor Corp.

K Number Device Name
K895999 PHOSPHORUS
K896000 ASPARTATE AMINOTRANFERASE (AST)
K896001 ALANINE AMINOTRANSFERASE (ALT)
K895423 ACCESS CHEMISTRY ANALYZER
K893137 EXCEL (TM) CHEMISTRY ANALYZER
K892331 ENZYMATIC UREA NITROGEN REAGENT SET
K893479 CHOLESTEROL REAGENT SET
K892002 NEOCHROME(R) III GLUCOSE
K890312 GAMMA-GLUTAMYLTRANSFERASE
K890034 PHOTOMETRIC METHOD, IRON (NON-HEME) (75JIY)
Search all 73 clearances from American Monitor Corp. →