KANIEVSKI SENSORY AID OR DEVICE— 510(k) K843433

Name: FDA 510(k) clearance K843433
Creator: U.S. Food and Drug Administration
Published: 1984-11-14

Substantially Equivalent

Spectro Industries, Inc.

FDA 510(k) clearance K843433 for KANIEVSKI SENSORY AID OR DEVICE, Substantially Equivalent on 1984-11-14. Applicant: Spectro Industries, Inc.. Device class: Unclassified.

Clearance details

Applicant: Spectro Industries, Inc.
Product code: Code LRA
Device class: Unclassified
Advisory panel: Unknown
Date received: 1984-09-04
Decision date: 1984-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jenkintown, PA, US

Download summary PDF View on FDA.gov ↗

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