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CARDIO REP RECOMBINANT CK ABNORMAL CONTROL

Page Type
Cleared 510(K)
510(k) Number
K932442
510(k) Type
Traditional
Applicant
HELENA LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1993
Days to Decision
161 days
Submission Type
Statement

CARDIO REP RECOMBINANT CK ABNORMAL CONTROL

Page Type
Cleared 510(K)
510(k) Number
K932442
510(k) Type
Traditional
Applicant
HELENA LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1993
Days to Decision
161 days
Submission Type
Statement