# K082902: RZ Endoscopic (Minimally Invasive) Instruments and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Rz Medizintechnik GmbH
- Decided: Dec 10, 2008 after 71 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.
No later device cites it as a predicate yet.
0 of 1 device 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) Jakoubek GmbH-manufactured predicate devices: named in the summary without a submission number
- (no number) Ackermann Instrumente GmbH-manufactured predicate devices: named in the summary without a submission number
- (no number) Gimmi GmbH-manufactured predicate devices: named in the summary without a submission number
- (no number) Pajunk GmbH-manufactured predicate devices: named in the summary without a submission number
- (no number) Sutter Medizintechnik GmbH-manufactured predicate devices: named in the summary without a submission number
- (no number) Guenter Bissinger Medizintechnik GmbH-manufactured predicate devices: named in the summary without a submission number

## Indications for use
RZ Endoscopic (Minimally Invasive) Instruments and Accessories are indicated for various endoscopic procedures and include both electrical and non-electrical accessories.

Source page: https://510kreport.com/device/K082902
Methodology: https://510kreport.com/methodology