MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149— 510(k) K001714

Name: FDA 510(k) clearance K001714
Creator: U.S. Food and Drug Administration
Published: 2000-11-03

Substantially Equivalent

Mercury Medical

FDA 510(k) clearance K001714 for MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149, Substantially Equivalent on 2000-11-03. Applicant: Mercury Medical. Device class: 2.

Clearance details

Applicant: Mercury Medical
Product code: Code NHK
Device class: Class 2
Regulation: 21 CFR 868.5905
Advisory panel: Anesthesiology
Date received: 2000-06-05
Decision date: 2000-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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