OTICON, E25P— 510(k) K830435

Substantially Equivalent

Octicon Corp.

FDA 510(k) clearance K830435 for OTICON, E25P, Substantially Equivalent on 1983-03-10. Applicant: Octicon Corp.. Device class: 1.

Clearance details

Applicant: Octicon Corp.
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1983-02-09
Decision date: 1983-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Octicon Corp.

K830436 — OTICON, E-27P1983-03-10

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