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SUTTER MODEL 10000 LEG CPM DEVICE

Page Type
Cleared 510(K)
510(k) Number
K914860
510(k) Type
Traditional
Applicant
SUTTER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1992
Days to Decision
71 days
Submission Type
Summary

SUTTER MODEL 10000 LEG CPM DEVICE

Page Type
Cleared 510(K)
510(k) Number
K914860
510(k) Type
Traditional
Applicant
SUTTER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1992
Days to Decision
71 days
Submission Type
Summary