# K093298: Pulsair Intellipuff, Pulsair Desktop Model 2414-P-2001, 2417-P-2000

- Pathway: 510(k) (Traditional)
- Applicant: Keeler Instruments, Inc.
- Decided: Dec 10, 2010 after 415 days
- Product code: HKX (Tonometer, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1930
- 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 K990257 (1999). 1 ancestor in all.
5 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990257: Keeler Pulsair 3000 Non Contact Tonometer, Keeler Instruments, Inc. (1999) Summary page 1.

## Most influential descendants
- K143086: VX120 Ophthalmic Diagnostic Device (2015), 3 descendants of its own
- K162067: VX130 Ophthalmic Diagnostic Device (2017), 1 descendant of its own
- K202221: VX650 (2021), 0 descendants of its own
- K201724: Pentacam AXL Wave (2020), 0 descendants of its own
- K181143: Keeler TonoCare Tonometer (2019), 0 descendants of its own

## Indications for use
The Pulsair IntelliPuff Non-Contact Tonometer is indicated for measuring intraocular pressure without contacting the eye to aid in the screening and diagnosis of glaucoma. The Pulsair Desktop Tonometer is indicated for measuring intraocular pressure without contacting the eye to aid in the screening and diagnosis of glaucoma.

Source page: https://510kreport.com/device/K093298
Methodology: https://510kreport.com/methodology