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MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882063
510(k) Type
Traditional
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1988
Days to Decision
28 days

MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882063
510(k) Type
Traditional
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1988
Days to Decision
28 days