# K041852: MR Tested Fiber Optic Short Laryngoscope Handle, Model 310002

- Pathway: 510(k) (Traditional)
- Applicant: Minrad, Inc.
- Decided: Nov 15, 2004 after 130 days
- Product code: CCW (Laryngoscope, Rigid)
- Device class: 1
- Regulation: 21 CFR 868.5540
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 3 cite 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)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K062523: Tru-MR Laryngoscope Set (2006), 2 descendants of its own
- K140951: Yeescope Laryngoscopes (2014), 0 descendants of its own
- K121378: Airtraq SP Airtraq Avant (2012), 0 descendants of its own
- K063477: Novamed Mri Conditional Laryngoscope Set (2007), 0 descendants of its own
- K062230: MR Fiber Optic Intubating Laryngoscope Handle, Short, Model 310002 (2006), 0 descendants of its own

## Indications for use
The MR Tested Fiber Optic Short Laryngoscope Handle ("MINRAD INC. MR Tested Fiber Optic Laryngoscepe Handle") is used, together with a Laryngoscope blade, to facilitate and aid in tracheal intubation in a Magnetic Resonance Imaging (MRI) or an interventional Magnetic Resonance (MR) environment, not to exceed a 1.5 Tesla static magnetic field.

Source page: https://510kreport.com/device/K041852
Methodology: https://510kreport.com/methodology