# K083840: Msi Medserv International-Rigid Endoscope

- Pathway: 510(k) (Traditional)
- Applicant: Msi Medserv International Deutschland GmbH
- Decided: Sep 28, 2009 after 278 days
- Product code: GCM (Endoscope, Rigid)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K950076 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K950076: Laparoscope, Olympus America, Inc. (1995) Summary page 4.

## Indications for use
MSI MedServ International Deutschland GmbH rigid endoscopes and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs and canals.

Source page: https://510kreport.com/device/K083840
Methodology: https://510kreport.com/methodology