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H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K946043
510(k) Type
Traditional
Applicant
RUDOLF RIESTER GMBH & CO. KG
Country
Germany
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/8/1995
Days to Decision
86 days
Submission Type
Statement

H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K946043
510(k) Type
Traditional
Applicant
RUDOLF RIESTER GMBH & CO. KG
Country
Germany
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/8/1995
Days to Decision
86 days
Submission Type
Statement