Edward Weck, Inc.
BOWIE-DICK TEST CARD CATALOG NUMBER 008018
SKU K897045UPC JOJ
In Stock
—
IIFDA 510(k) Cleared (K897045)
1
Free shipping on orders over $99 · 30-day returns
Edward Weck, Inc.
Free shipping on orders over $99 · 30-day returns
BOWIE-DICK TEST CARD CATALOG NUMBER 008018 is an FDA 510(k)-cleared medical device (K897045) manufactured by Edward Weck, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 14, 1990. Regulation: 8.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
McKesson
SKU VM-1270030
Hollister
SKU VM-1270031