# K082197: Rhytec, Inc., Portrait PSR

- Pathway: 510(k) (Special)
- Applicant: Rhytec Incorporated
- Decided: Aug 22, 2008 after 18 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: 15 generations back to K943450 (1995). 147 ancestors in all.
3 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)
- K073111: Portrait PSR, Model 745915, Rhytec Incorporated (2008) Summary page 1.

## Most influential descendants
- 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 System is indicated for treatment of the following dermatological conditions: • Treatment of wrinkles and rhytides • Superficial skin lesions • Actinic keratosis • Viral papillomata • Seborrhoeic keratosis • Acne scars

Source page: https://510kreport.com/device/K082197
Methodology: https://510kreport.com/methodology