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

AMERICAN MONITOR MAGNESIUM #'S 1036&4021

K Number: K802091 · Decision Oct 10, 1980
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
73
Review Days
38

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Basic Information

Device Name
AMERICAN MONITOR MAGNESIUM #'S 1036&4021
K Number
K802091
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Monitor Corp.
Date Received
September 2, 1980
Decision Date
October 10, 1980
Product Code
JGJ
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
JGJ Photometric Method, Magnesium

Similar 510(k) Clearances

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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. →