SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS— 510(k) K921863
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K921863 for SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS, Substantially Equivalent on 1992-09-28. Applicant: Hewlett-Packard Co.. Device class: 2.
Clearance details
- Applicant
- Hewlett-Packard Co.
- Product code
- Code GXW
- Device class
- Class 2
- Regulation
- 21 CFR 882.1240
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.