Last synced on 14 November 2025 at 11:06 pm

GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISK

Page Type
Cleared 510(K)
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)
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