# K032822: Asap Sinuscope 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0

- Pathway: 510(k) (Traditional)
- Applicant: Asap Endoscopic Products GmbH
- Decided: Jan 8, 2004 after 120 days
- Product code: EOB (Nasopharyngoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K874215 (1988). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981751: Sinuscope and Accessories, Henke Sass Wolf of America, Inc. (1998) Summary page 1.

## Most influential descendants
- K082667: Visionsense Stereoscopic Vision System (VS System) (2008), 1 descendant of its own
- K162410: TIPCAM 1S 3D System (2017), 0 descendants of its own

## Indications for use
The asap ENT endoscope is intended to provide the physician with a means for direct viewing of the nasal cavity and nasal pharynx by providing illumination and visualization of these regions during various diagnostic and therapeutic procedures. The asap ENT endoscope is reusable.

Source page: https://510kreport.com/device/K032822
Methodology: https://510kreport.com/methodology