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AMERLITE TSH-30 ULTRASENSITIVE ASSAY (LAN.0010Q/2010Q)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952211
510(k) Type
Traditional
Applicant
JOHNSON & JOHNSON CLINICAL DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1995
Days to Decision
64 days
Submission Type
Statement

AMERLITE TSH-30 ULTRASENSITIVE ASSAY (LAN.0010Q/2010Q)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952211
510(k) Type
Traditional
Applicant
JOHNSON & JOHNSON CLINICAL DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1995
Days to Decision
64 days
Submission Type
Statement