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GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851228
510(k) Type
Traditional
Applicant
WARNER-LAMBERT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/1985
Days to Decision
29 days

GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851228
510(k) Type
Traditional
Applicant
WARNER-LAMBERT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/1985
Days to Decision
29 days