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MODIFIED AMERLEX-M PROGESTERONE RADIOIMMUNO. KIT

Page Type
Cleared 510(K)
510(k) Number
K880934
510(k) Type
Traditional
Applicant
AMERSHAM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1988
Days to Decision
42 days

MODIFIED AMERLEX-M PROGESTERONE RADIOIMMUNO. KIT

Page Type
Cleared 510(K)
510(k) Number
K880934
510(k) Type
Traditional
Applicant
AMERSHAM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1988
Days to Decision
42 days