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DIGISTIM II

Page Type
Cleared 510(K)
510(k) Number
K822137
510(k) Type
Traditional
Applicant
BEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1982
Days to Decision
11 days

DIGISTIM II

Page Type
Cleared 510(K)
510(k) Number
K822137
510(k) Type
Traditional
Applicant
BEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1982
Days to Decision
11 days