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SONICAID FM820, SONICAID FM830

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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