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REPROCESSED RF ARTHROSCOPY PROBES

Page Type
Cleared 510(K)
510(k) Number
K012679
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2001
Days to Decision
86 days
Submission Type
Summary

REPROCESSED RF ARTHROSCOPY PROBES

Page Type
Cleared 510(K)
510(k) Number
K012679
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2001
Days to Decision
86 days
Submission Type
Summary