MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX— 510(k) K954492

Name: FDA 510(k) clearance K954492
Creator: U.S. Food and Drug Administration
Published: 1996-10-21

Substantially Equivalent

Mercury Medical

FDA 510(k) clearance K954492 for MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX, Substantially Equivalent on 1996-10-21. Applicant: Mercury Medical. Device class: 2.

Clearance details

Applicant: Mercury Medical
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1995-09-27
Decision date: 1996-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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