VERIL/PPR PERSONAL PAIN RELIEVER #800— 510(k) K822929

Substantially Equivalent

Verite

FDA 510(k) clearance K822929 for VERIL/PPR PERSONAL PAIN RELIEVER #800, Substantially Equivalent on 1982-11-17. Applicant: Verite. Device class: 2.

Clearance details

Applicant: Verite
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1982-10-04
Decision date: 1982-11-17
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

K844727 — MODEL 10001985-07-09
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K820651 — MODEL 860-1 VERI/PROBE1982-04-29
K813108 — MODEL 500 VERI/5001982-02-19

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