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DURADERM BUTTERFLY

Page Type
Cleared 510(K)
510(k) Number
K881343
510(k) Type
Traditional
Applicant
SENTRY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1988
Days to Decision
35 days

DURADERM BUTTERFLY

Page Type
Cleared 510(K)
510(k) Number
K881343
510(k) Type
Traditional
Applicant
SENTRY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1988
Days to Decision
35 days