Last synced on 30 November 2024 at 11:09 am

AESCULAP ANGLED NEUROENDOSCOPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964281
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1997
Days to Decision
175 days
Submission Type
Summary

AESCULAP ANGLED NEUROENDOSCOPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964281
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1997
Days to Decision
175 days
Submission Type
Summary