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

MAGNESIUM TEST ITEM NUMBER: 65419

K Number: K894508 · Decision Aug 31, 1989
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
288
Review Days
43

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Basic Information

Device Name
MAGNESIUM TEST ITEM NUMBER: 65419
K Number
K894508
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Em Diagnostic Systems, Inc.
Date Received
July 19, 1989
Decision Date
August 31, 1989
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

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Other Clearances by Em Diagnostic Systems, Inc.

K Number Device Name
K935181 ASPARTATE AMINOTRANSFERASE (AST) TEST
K935180 ALANINE AMINOTRANSFERASE (ALT) TEST
K935178 EMDS PHOSPHOROUS (PHOS) TEST
K935179 EMDS ALBUMIN (ALB) TEST
K935174 TOTAL PROTEIN TEST (TPRO)
K935177 GAMMA-GLUTAMYL TRANSFERASE (GGT) TEST
K935136 CHOLESTEROL (CHOL) TEST ITEM NO. 65410
K935175 LACTATE DEHYDROGENASE (LD)
K935176 IRON TEST
K935183 EMDS MAGNESIUM (MG) TEST
Search all 288 clearances from Em Diagnostic Systems, Inc. →