Angiosystems, Inc.
PROCEDURE KIT/ROUTINE DENTAL PROCEDURES
SKU K905461UPC EKS
In Stock
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IFDA 510(k) Cleared (K905461)
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Free shipping on orders over $99 · 30-day returns
Angiosystems, Inc.
Free shipping on orders over $99 · 30-day returns
PROCEDURE KIT/ROUTINE DENTAL PROCEDURES is an FDA 510(k)-cleared medical device (K905461) manufactured by Angiosystems, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 4, 1991. Regulation: 8.
