Last synced on 23 September 2022 at 11:05 pm

FOOT VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790195
510(k) Type
Traditional
Applicant
AMERICAN SAFETY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1979
Days to Decision
33 days

FOOT VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790195
510(k) Type
Traditional
Applicant
AMERICAN SAFETY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1979
Days to Decision
33 days