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KRATZ NOVA SERT(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883489
510(k) Type
Traditional
Applicant
COOPERVISION-CILCO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1988
Days to Decision
70 days

KRATZ NOVA SERT(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883489
510(k) Type
Traditional
Applicant
COOPERVISION-CILCO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1988
Days to Decision
70 days