# K141046: Midi-SRS

- Pathway: 510(k) (Traditional)
- Applicant: Srmc Co., Ltd.
- Decided: Dec 24, 2014 after 245 days
- Product code: ONG (Powered Laser Surgical Instrument With MicrobeamFractional Output)
- 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 K080382 (2008). 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)
- K080382: Sellas, Dinona Co., Ltd. (2008) Summary page 4.

## Indications for use
MiDi-SRS is intended for use in dermatological procedures requiring the coagulation of soft tissue.

Source page: https://510kreport.com/device/K141046
Methodology: https://510kreport.com/methodology