Medi Nuclear Corp., Inc.
NEBULIZER (DIRECT PATIENT INTERFACE)
SKU K915075UPC CAF
In Stock
—
IIFDA 510(k) Cleared (K915075)
1
Free shipping on orders over $99 · 30-day returns
Medi Nuclear Corp., Inc.
Free shipping on orders over $99 · 30-day returns
NEBULIZER (DIRECT PATIENT INTERFACE) is an FDA 510(k)-cleared medical device (K915075) manufactured by Medi Nuclear Corp., Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 1992. Regulation: 8.
ADC
SKU DX606933
MDF
SKU DX683863
3M Littmann
SKU DX771242
Welch Allyn
SKU DX297280