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SONICAID FM820, SONICAID FM830

Page Type
Cleared 510(K)
510(k) Number
K002150
510(k) Type
Traditional
Applicant
OXFORD INSTRUMENTS
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/9/2001
Days to Decision
235 days
Submission Type
Statement

SONICAID FM820, SONICAID FM830

Page Type
Cleared 510(K)
510(k) Number
K002150
510(k) Type
Traditional
Applicant
OXFORD INSTRUMENTS
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/9/2001
Days to Decision
235 days
Submission Type
Statement