Last synced on 4 February 2023 at 10:33 pm

MEDITEC LINK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981196
510(k) Type
Traditional
Applicant
AESCULAP-MEDITEC NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1998
Days to Decision
90 days
Submission Type
Summary

MEDITEC LINK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981196
510(k) Type
Traditional
Applicant
AESCULAP-MEDITEC NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1998
Days to Decision
90 days
Submission Type
Summary