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B&R DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032925
510(k) Type
Traditional
Applicant
RONVIG A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
12/22/2003
Days to Decision
91 days
Submission Type
Statement

B&R DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032925
510(k) Type
Traditional
Applicant
RONVIG A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
12/22/2003
Days to Decision
91 days
Submission Type
Statement