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PERI-GUARD PERICARDIAL PATCH-HERNIA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833021
510(k) Type
Traditional
Applicant
GENETIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/26/1983
Days to Decision
111 days

PERI-GUARD PERICARDIAL PATCH-HERNIA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833021
510(k) Type
Traditional
Applicant
GENETIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/26/1983
Days to Decision
111 days