# K982965: Endocam Camera Systems 5502/5507 with CR Camera Heads and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Nov 23, 1998 after 90 days
- Product code: FWF (Camera, Television, Endoscopic, Without Audio)
- Device class: 1
- Regulation: 21 CFR 878.4160
- 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 K942817 (1994). 2 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K950502: CCD Endocam 5501, Richard Wolf Medical Instruments Corp. (1995) Summary page 1.
- K942817: CCD Endocam Office 5510, Richard Wolf Medical Instruments Corp. (1994) Summary page 1.

## Most influential descendants
- K023659: 1-CCD Endocam 5520 System (2003), 10 descendants of its own
- K080977: 3 CCD Endocam 5550 (2008), 7 descendants of its own
- K130423: The Richard Wolf Endocam Logic HD Camera System 5525 (2013), 6 descendants of its own
- K180583: Logic 4K Camera Controller, Logic 4K Camera Head (2018), 4 descendants of its own
- K200617: Logic HD Camera Controller, Logic HD Lite Camera Controller, Logic 4K Camera Contoller, Adapter for Controller 5525 (2020), 2 descendants of its own

## Indications for use
The 1 CCD Endocam 5502 and 3 CCD Endocam 5507 are designed for video endoscopy and video microscopy and can be used for both diagnostic and therapeutic interventions. The camera head is classified as Cardiac Floating (CF) equipment with less than 10pA of leakage current. This permits its use for cardiac visualization procedures when used in conjunction with the proper instrumentation for entry into the cardiac system.

Source page: https://510kreport.com/device/K982965
Methodology: https://510kreport.com/methodology