# Cavitron Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 32 (1976–1981): 32 510(k) clearances
- Product codes: CCK (3), EHL (3), HQB (2), ELC (2), HPT (2), BZC (2), DXN (1), HQF (1), CCL (1), CHL (1), EID (1), GEI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Radionics, A Division of Tyco Healthcare Group LP: 1 (https://510kreport.com/company/radionics-a-division-of-tyco-healthcare-group)
- Misonix, Inc.: 1 (https://510kreport.com/company/misonix)
- Ultralase Technologies, Inc.: 1 (https://510kreport.com/company/ultralase-technologies)
- Olympus Optical Co., Ltd.: 1 (https://510kreport.com/company/olympus-optical)

## Its most-cited devices
- K801623: Cavitron Ultrasonic Surg. Aspir. Cusa (1980), cited by 4

## Recent decisions
- K811582: The Placer (Jul 28, 1981)
- K810207: Minor Surgery Light (Feb 13, 1981)
- K802928: Spirometric Computer #SC-10 (Dec 17, 1980)
- K801623: Cavitron Ultrasonic Surg. Aspir. Cusa (Nov 18, 1980)
- K801877: Slit Lamp Attachment (Sep 16, 1980)
- K800869: Model PM-20(N)(R)CO2 Patient Monitor/Ala (May 28, 1980)
- K800722: Auto-Field D Automated Visual Detector (Apr 29, 1980)
- K791585: Model G-61 Ultrasonic Dental Unit (Sep 19, 1979)

Source page: https://510kreport.com/company/cavitron