OLYMPIA FACEPLATE MODULE— 510(k) K896304

Name: FDA 510(k) clearance K896304
Creator: U.S. Food and Drug Administration
Published: 1990-01-26

Substantially Equivalent

Olympia Instruments, Inc.

FDA 510(k) clearance K896304 for OLYMPIA FACEPLATE MODULE, Substantially Equivalent on 1990-01-26. Applicant: Olympia Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Olympia Instruments, Inc.
Product code: Code LRB
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1989-10-30
Decision date: 1990-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Longwood, FL, US

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