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PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE

Page Type
Cleared 510(K)
510(k) Number
K962903
510(k) Type
Traditional
Applicant
PRESTIGE MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1998
Days to Decision
586 days
Submission Type
Summary

PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE

Page Type
Cleared 510(K)
510(k) Number
K962903
510(k) Type
Traditional
Applicant
PRESTIGE MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1998
Days to Decision
586 days
Submission Type
Summary