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KERAVISION VACUUM RING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984540
510(k) Type
Abbreviated
Applicant
KERAVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1999
Days to Decision
128 days
Submission Type
Summary

KERAVISION VACUUM RING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984540
510(k) Type
Abbreviated
Applicant
KERAVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1999
Days to Decision
128 days
Submission Type
Summary