A SLEEP ASSESSMENT DEVICE— 510(k) K792305

Substantially Equivalent

Farrall Instruments, Inc.

FDA 510(k) clearance K792305 for A SLEEP ASSESSMENT DEVICE, Substantially Equivalent on 1979-12-20. Applicant: Farrall Instruments, Inc..

Clearance details

Applicant: Farrall Instruments, Inc.
Product code: Code LEL
Advisory panel: Neurology
Date received: 1979-11-16
Decision date: 1979-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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