NEEDLE HOLDERS— 510(k) K822197

Substantially Equivalent

Kelleher Corp.

FDA 510(k) clearance K822197 for NEEDLE HOLDERS, Substantially Equivalent on 1982-08-16. Applicant: Kelleher Corp.. Device class: 2.

Clearance details

Applicant: Kelleher Corp.
Product code: Code LCR
Device class: Class 2
Regulation: 21 CFR 862.3900
Advisory panel: Clinical Toxicology
Date received: 1982-07-23
Decision date: 1982-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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