Last synced on 25 November 2022 at 11:04 pm

WILLIAMS OESOPHAGEAL VARICES INJECT TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810180
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1981
Days to Decision
18 days

WILLIAMS OESOPHAGEAL VARICES INJECT TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810180
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1981
Days to Decision
18 days