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REPROCESSED VESSEL SEALER

Page Type
Cleared 510(K)
510(k) Number
K123096
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2013
Days to Decision
115 days
Submission Type
Summary

REPROCESSED VESSEL SEALER

Page Type
Cleared 510(K)
510(k) Number
K123096
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2013
Days to Decision
115 days
Submission Type
Summary