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INTRASITE GEL (LABELING REVISION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904411
510(k) Type
Traditional
Applicant
SMITH & NEPHEW UNITED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/26/1990
Days to Decision
61 days

INTRASITE GEL (LABELING REVISION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904411
510(k) Type
Traditional
Applicant
SMITH & NEPHEW UNITED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/26/1990
Days to Decision
61 days