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MEROCEL INSTRUMENT WIPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791736
510(k) Type
Traditional
Applicant
XOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1979
Days to Decision
19 days

MEROCEL INSTRUMENT WIPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791736
510(k) Type
Traditional
Applicant
XOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1979
Days to Decision
19 days