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MODIFIED KEYMED FLEXIBLE ESOPHAGEAL DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881478
510(k) Type
Traditional
Applicant
KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT), LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/14/1988
Days to Decision
161 days

MODIFIED KEYMED FLEXIBLE ESOPHAGEAL DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881478
510(k) Type
Traditional
Applicant
KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT), LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/14/1988
Days to Decision
161 days