MONOPOLAR INJECTION NEEDLE ELECTRODE— 510(k) K854793

Name: FDA 510(k) clearance K854793
Creator: U.S. Food and Drug Administration
Published: 1986-02-18

Substantially Equivalent for Some Indications

Oculinum, Inc.

FDA 510(k) clearance K854793 for MONOPOLAR INJECTION NEEDLE ELECTRODE, Substantially Equivalent for Some Indications on 1986-02-18. Applicant: Oculinum, Inc.. Device class: 2.

Clearance details

Applicant: Oculinum, Inc.
Product code: Code HLW
Device class: Class 2
Regulation: 21 CFR 886.1640
Advisory panel: Ophthalmic
Date received: 1985-12-05
Decision date: 1986-02-18
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Mill Valley, CA, US

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K900279 — OCULINUM INJECTION AMPLIFIER1990-02-09

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