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KERAVISION VACUUM RING SYSTEM

Page Type
Cleared 510(K)
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)
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