Last synced on 16 August 2024 at 11:05 pm

AESCULAP TROCAR INSTRUMENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934724
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/1993
Days to Decision
83 days
Submission Type
Summary

AESCULAP TROCAR INSTRUMENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934724
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/1993
Days to Decision
83 days
Submission Type
Summary