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VISIO-BOND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790833
510(k) Type
Traditional
Applicant
ESPE GMBH (US)
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
4/30/1979
Days to Decision
0 days

VISIO-BOND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790833
510(k) Type
Traditional
Applicant
ESPE GMBH (US)
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
4/30/1979
Days to Decision
0 days