Last synced on 25 January 2026 at 3:41 am

SONICAID FM820, SONICAID FM830

Page Type
Cleared 510(K)
PDF
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
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