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PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890182
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1990
Days to Decision
406 days

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890182
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1990
Days to Decision
406 days