# K000767: Memcath Urology Introducer Sheath, Model 201

- Pathway: 510(k) (Traditional)
- Applicant: Memcath Technologies, LLC
- Decided: Jun 5, 2000 after 88 days
- Product code: KNY (Accessories, Catheter, G-U)
- Device class: 2
- Regulation: 21 CFR 876.5130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K061663: Endomedical Technologies Quik-Cover Flexible Endoscope Barrier Sheath for Otolaryngoscopes and Bronchoscopes (2006), 0 descendants of its own
- K061324: Emt Quik-Cover Flexible Endoscope Barrier Sheath, Series 1-7 (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K000767
Methodology: https://510kreport.com/methodology