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KEYMED FLEXIBLE ESOPHAGEAL DILATORS

Page Type
Cleared 510(K)
510(k) Number
K862000
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/12/1986
Days to Decision
81 days

KEYMED FLEXIBLE ESOPHAGEAL DILATORS

Page Type
Cleared 510(K)
510(k) Number
K862000
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/12/1986
Days to Decision
81 days