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MICRO CISE DIAMOND SCALPEL

Page Type
Cleared 510(K)
510(k) Number
K820730
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/9/1982
Days to Decision
23 days

MICRO CISE DIAMOND SCALPEL

Page Type
Cleared 510(K)
510(k) Number
K820730
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/9/1982
Days to Decision
23 days