# K071786: Portrait PSR

- Pathway: 510(k) (Special)
- Applicant: Rhytec Incorporated
- Decided: Jul 26, 2007 after 24 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: 13 generations back to K943450 (1995). 30 ancestors in all.
109 later devices descend from it; 2 cite it directly.
0 of 140 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060948: Portrait PSR3, Rhytec Incorporated (2006) Summary page 1.

## Most influential descendants
- K072394: Portrait Stand-Off (2007), 104 descendants of its own
- K073572: Matrix RF Applicator (2008), 102 descendants of its own
- K101510: Fractional Skin Resurfacing (FSR) Applicator (2011), 64 descendants of its own
- K130501: Intensif (2014), 57 descendants of its own
- K180189: InMode System with Fractora3D/3D-90 Applicators (2018), 38 descendants of its own

## Indications for use
The Portrait® PSR 3 is indicated for treatment of the following dermatological conditions: Treatment of wrinkles and rhytides Superficial skin lesions Actinic Keratosis Viral Papillomata Seborrhoeic Keratosis

Source page: https://510kreport.com/device/K071786
Methodology: https://510kreport.com/methodology