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THE KEYMED FIBERSCOPE STERILIZATION CASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860528
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/15/1986
Days to Decision
154 days

THE KEYMED FIBERSCOPE STERILIZATION CASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860528
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/15/1986
Days to Decision
154 days