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

EMDS(TM) LACTIC DEHYDROGENASE TESTPACKS, #67660/95

K Number: K863477 · Decision Sep 26, 1986
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
110
Applicant Total
288
Review Days
17

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EMDS(TM) LACTIC DEHYDROGENASE TESTPACKS, #67660/95
K Number
K863477
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1440
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Em Diagnostic Systems, Inc.
Date Received
September 9, 1986
Decision Date
September 26, 1986
Product Code
CFJ
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
CFJ Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase

Similar 510(k) Clearances

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

View all

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. →