MODEL 500 VERI/500— 510(k) K813108

Substantially Equivalent

Verite

FDA 510(k) clearance K813108 for MODEL 500 VERI/500, Substantially Equivalent on 1982-02-19. Applicant: Verite. Device class: 2.

Clearance details

Applicant: Verite
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1981-11-03
Decision date: 1982-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Verite

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K822929 — VERIL/PPR PERSONAL PAIN RELIEVER #8001982-11-17
K820651 — MODEL 860-1 VERI/PROBE1982-04-29

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