PEAK FLOW RATE METER— 510(k) K893827

Substantially Equivalent

Laytech Medical Co.

FDA 510(k) clearance K893827 for PEAK FLOW RATE METER, Substantially Equivalent on 1989-08-11. Applicant: Laytech Medical Co.. Device class: 2.

Clearance details

Applicant: Laytech Medical Co.
Product code: Code FFG
Device class: Class 2
Regulation: 21 CFR 876.1800
Advisory panel: Gastroenterology, Urology
Date received: 1989-05-24
Decision date: 1989-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.