# K933157: Erbotom Icc 200

- Pathway: 510(k) (Traditional)
- Applicant: Erbe USA, Inc.
- Decided: Feb 23, 1994 after 239 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
No predicates in its family tree.
144 later devices descend from it; 8 cite it directly.
0 of 145 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) ACC 450: named in the summary without a submission number

## Most influential descendants
- K013255: Surgitron 120 Iec (Also Known as Surgitron 4.0 Dual RF (2001), 104 descendants of its own
- K082834: Ellman International Non-Ablative Technique for Surgitron  Iec (2009), 56 descendants of its own
- K101967: Non-Ablative Wrinkle Treatent Handpiece Modle Pelleve' (2010), 53 descendants of its own
- K102368: Non-Ablative Wrinkle Treatment Handpiece (2010), 52 descendants of its own
- K102698: Pelleve Glidesafe Non-Ablative Wrinkle Treatment System Model Pelleve Glidesafe (2011), 39 descendants of its own

Source page: https://510kreport.com/device/K933157
Methodology: https://510kreport.com/methodology