A SLEEP ASSESSMENT DEVICE— 510(k) K792305
Substantially EquivalentFarrall Instruments, Inc.
FDA 510(k) clearance K792305 for A SLEEP ASSESSMENT DEVICE, Substantially Equivalent on 1979-12-20. Applicant: Farrall Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Farrall Instruments, Inc.
- Product code
- Code LEL
- Device class
- Class 2
- Regulation
- 21 CFR 882.5050
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code LEL
view allMore clearances from Farrall Instruments, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.