# Sonicaid, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 18 (1977–1988): 18 510(k) clearances
- Product codes: HGM (3), JOM (2), KNG (2), JOP (2), HEM (1), DPT (1), KXO (1), DPW (1), LBA (1), DQB (1), ITX (1), HFO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K873673: BV105 (&BV105R) Vascular Flow Detector W/Optional (Feb 26, 1988)
- K872074: 5 MHZ Transducer (Aug 25, 1987)
- K863803: Vasopulse (TM)/Model 5000 (May 6, 1987)
- K862720: Vasoflo-3 & Extravascular Blood Flow Probes (Nov 17, 1986)
- K861237: Vasoview Duplex Imaging System (Jul 14, 1986)
- K851102: Vasoscreen Impedance Plethysmograph (May 16, 1985)
- K833902: Vasoscan (Jan 27, 1984)
- K832374: Photoflo Dual-Mode Photoplethysmograph (Dec 1, 1983)

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