NIOX ARTICLE NO: 02-1000— 510(k) DEN030001

Unknown

Aerocrine AB

FDA 510(k) clearance DEN030001 for NIOX ARTICLE NO: 02-1000, Unknown on 2003-04-30. Applicant: Aerocrine AB. Device class: 2.

Clearance details

Applicant: Aerocrine AB
Product code: Code MXA
Device class: Class 2
Regulation: 21 CFR 862.3080
Advisory panel: Clinical Toxicology
Date received: 2003-03-18
Decision date: 2003-04-30
Decision: Unknown
Clearance type: Post-NSE
Location: San Diego, CA, US

View on FDA.gov ↗

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