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DE LUXE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925755
510(k) Type
Traditional
Applicant
RUDOLF RIESTER GMBH & CO. KG
Country
Germany
FDA Decision
Substantially Equivalent - Kit
Decision Date
12/3/1993
Days to Decision
385 days
Submission Type
Statement

DE LUXE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925755
510(k) Type
Traditional
Applicant
RUDOLF RIESTER GMBH & CO. KG
Country
Germany
FDA Decision
Substantially Equivalent - Kit
Decision Date
12/3/1993
Days to Decision
385 days
Submission Type
Statement