Last synced on 18 April 2025 at 11:05 pm

ZEST PLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801524
510(k) Type
Traditional
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1980
Days to Decision
20 days

ZEST PLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801524
510(k) Type
Traditional
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1980
Days to Decision
20 days