Last synced on 14 November 2025 at 11:06 pm

AMERLITE PROGESTERONE ASSAY, LAN.0079/2079 240/144

Page Type
Cleared 510(K)
510(k) Number
K884100
510(k) Type
Traditional
Applicant
AMERSHAM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1988
Days to Decision
43 days

AMERLITE PROGESTERONE ASSAY, LAN.0079/2079 240/144

Page Type
Cleared 510(K)
510(k) Number
K884100
510(k) Type
Traditional
Applicant
AMERSHAM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1988
Days to Decision
43 days