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REPROCESSED SURGICAL ELECTRIC INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K120040
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2012
Days to Decision
274 days
Submission Type
Summary

REPROCESSED SURGICAL ELECTRIC INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K120040
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2012
Days to Decision
274 days
Submission Type
Summary