Sentek, Inc.
REVISED T-SCAN SYSTEM
SKU K870032UPC EFH
In Stock
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IFDA 510(k) Cleared (K870032)
1
Free shipping on orders over $99 · 30-day returns
Sentek, Inc.
Free shipping on orders over $99 · 30-day returns
REVISED T-SCAN SYSTEM is an FDA 510(k)-cleared medical device (K870032) manufactured by Sentek, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 1, 1987. Regulation: 8.
