Last synced on 16 May 2025 at 11:05 pm

CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980961
510(k) Type
Traditional
Applicant
CORDIS WEBSTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1998
Days to Decision
73 days
Submission Type
Summary

CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980961
510(k) Type
Traditional
Applicant
CORDIS WEBSTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1998
Days to Decision
73 days
Submission Type
Summary