# K073111: Portrait PSR, Model 745915

- Pathway: 510(k) (Traditional)
- Applicant: Rhytec Incorporated
- Decided: Mar 27, 2008 after 143 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K943450 (1995). 146 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 151 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071786: Portrait PSR, Rhytec Incorporated (2007) Summary page 1.
- K963339: Coherent Ultrapulse CO2 Surgical Lasers, Coherent Medical Group (1997) Summary page 1.
- K030453: Cooltouch ND: Yag Laser System, New Star Lasers, Inc. (2003) Summary page 1.
- K053047: Fraxel SR Laser System, Reliant Technologies, Inc. (2006) Summary page 1.

## Most influential descendants
- K082197: Rhytec, Inc., Portrait PSR (2008), 3 descendants of its own
- K132754: Neogen PSR System (2013), 2 descendants of its own
- K221873: NeoGen PSR System (2023), 0 descendants of its own
- K211652: Renuvion Dermal Handpiece, Renuvion Dermal System (2022), 0 descendants of its own

## Indications for use
The Portrait® PSR 3 is intended for treatment of the following dermatological conductions: 1. Treatment of wrinkles and rhytides 2. Superficial skin lesions 3. Actinic keratosis 4. Viral papillomata 5. Seborrhoeic keratosis 6. Acne Scars

Source page: https://510kreport.com/device/K073111
Methodology: https://510kreport.com/methodology