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CLINIC 2000 MODEL MULTI-FRECODYN DEVICE

Page Type
Cleared 510(K)
510(k) Number
K820784
510(k) Type
Traditional
Applicant
DIMECO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1982
Days to Decision
30 days

CLINIC 2000 MODEL MULTI-FRECODYN DEVICE

Page Type
Cleared 510(K)
510(k) Number
K820784
510(k) Type
Traditional
Applicant
DIMECO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1982
Days to Decision
30 days