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DISPOSABLE OCUTOME PROBE

Page Type
Cleared 510(K)
510(k) Number
K833371
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/4/1984
Days to Decision
99 days

DISPOSABLE OCUTOME PROBE

Page Type
Cleared 510(K)
510(k) Number
K833371
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/4/1984
Days to Decision
99 days