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CYSTOTOMES/KNIFES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880345
510(k) Type
Traditional
Applicant
MYOCURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1988
Days to Decision
98 days

CYSTOTOMES/KNIFES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880345
510(k) Type
Traditional
Applicant
MYOCURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1988
Days to Decision
98 days