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

TITAN GEL CPK REP SYSTEM

K Number: K873399 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
280
Review Days
57

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Basic Information

Device Name
TITAN GEL CPK REP SYSTEM
K Number
K873399
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Helena Laboratories
Date Received
August 24, 1987
Decision Date
October 20, 1987
Product Code
JHX
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
JHX Fluorometric Method, Cpk Or Isoenzymes

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Other Clearances by Helena Laboratories

K Number Device Name
K131479 V8 SP NORMAL CONTROL, ABNORMAL CONTROL
K100103 SPECIALTY ASSAYED CONTROL-2
K061991 PLATELETWORKS ARACHIDONIC ACID, MODEL PW-ACA
K061069 SPIFE IFE-15 PENTAVALENT, MODEL 3456, SPIFE IFE-9 PENTAVALENT KIT, MODEL 3457, SPIFT IFE-6 PENTAVALENT KIT, MODEL 3458
K061014 ACTALYKE QC KIT, MODELS AQC-HP AND AQC-LP
K050053 HEMORAM/AGGRAM ANALYZER
K024162 SPIFE 3000 TITAN GEL IGG IEF KIT, MODEL 3389
K023761 PLATELETWORKS, MODELS PW-A, PW-C
K022757 SPIFE CK KIT, MODEL 3332, 3333
K022455 SPIFE LD-12 KIT, MODEL 3338
Search all 280 clearances from Helena Laboratories →