# K984486: Pulsemaster Dental Laser System

- Pathway: 510(k) (Traditional)
- Applicant: American Dental Technologies, Inc.
- Decided: May 13, 1999 after 147 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K932683 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K932683: Centauri, Premier Laser Systems, Inc. (1997) Summary page 1.
- (no number) High Speed Dental Handpieces: named in the summary without a submission number

## Indications for use
The American Dental Technologies, Inc. PulseMaster Dental Laser Systems are indicated for use for selective ablation of enamel (first degree) dental caries.

Source page: https://510kreport.com/device/K984486
Methodology: https://510kreport.com/methodology