Gn Danavox, Inc.
143 SERIES BTE
SKU K905692UPC ESD
In Stock
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IFDA 510(k) Cleared (K905692)
1
Free shipping on orders over $99 · 30-day returns
Gn Danavox, Inc.
Free shipping on orders over $99 · 30-day returns
143 SERIES BTE is an FDA 510(k)-cleared medical device (K905692) manufactured by Gn Danavox, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 27, 1991. Regulation: 8.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
McKesson
SKU VM-1270030
Hollister
SKU VM-1270031