# K181456: Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves

- Pathway: 510(k) (Traditional)
- Applicant: Tuttnauer, Ltd.
- Decided: Jul 8, 2019 after 399 days
- Product code: FLE (Sterilizer, Steam)
- Device class: 2
- Regulation: 21 CFR 880.6880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K221227: Tuttnauer Horizontal autoclave series model: 4472, 5596, 6690, 66120 (2022), 0 descendants of its own

## Indications for use
The Tuttnauer Horizontal Models: 4472,5596,6690, 6990, 66120, 69120 and 69180 autoclaves that are intended for use by a health care providers to sterilize medical products by means of pressurized steam. The devices are autoclaves are intended to provide sterilization of heat stable medical devices; wrapped solids, hollow and porous products.

Source page: https://510kreport.com/device/K181456
Methodology: https://510kreport.com/methodology