# K961136: Pulsemaster

- Pathway: 510(k) (Traditional)
- Applicant: American Dental Technologies, Inc.
- Decided: Jun 3, 1996 after 74 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
No predicates in its family tree.
209 later devices descend from it; 1 cites it directly.
0 of 210 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) PulseMaster laser: named in the summary without a submission number

## Most influential descendants
- K983058: Ceralas D Laser System, Model # Ceralas D15 (1998), 208 descendants of its own
- K991891: Ceralas Diode Laser System, Model Ceralas D15 (1999), 207 descendants of its own
- K072779: Ceralas D 980NM Diode Laser, Models D15 and D25 (2008), 153 descendants of its own
- K081352: Profile Multi-Platform System (2008), 112 descendants of its own
- K101916: Joule Multi-Platform System (2011), 111 descendants of its own

## Indications for use
Aphthous Ulcers

Source page: https://510kreport.com/device/K961136
Methodology: https://510kreport.com/methodology