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SUTTER MODEL 6000 HAND CPM DEVICE

Page Type
Cleared 510(K)
510(k) Number
K945221
510(k) Type
Traditional
Applicant
SUTTER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1995
Days to Decision
124 days
Submission Type
Summary

SUTTER MODEL 6000 HAND CPM DEVICE

Page Type
Cleared 510(K)
510(k) Number
K945221
510(k) Type
Traditional
Applicant
SUTTER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1995
Days to Decision
124 days
Submission Type
Summary