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SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880758
510(k) Type
Traditional
Applicant
BOOTS-CELLTECH DIAGNOSTICS, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/18/1988
Days to Decision
53 days

SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880758
510(k) Type
Traditional
Applicant
BOOTS-CELLTECH DIAGNOSTICS, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/18/1988
Days to Decision
53 days