RESPITRACE PLUS— 510(k) K894973

Substantially Equivalent

Hogan & Hartson

FDA 510(k) clearance K894973 for RESPITRACE PLUS, Substantially Equivalent on 1989-10-30. Applicant: Hogan & Hartson. Device class: 2.

Clearance details

Applicant: Hogan & Hartson
Product code: Code FLS
Device class: Class 2
Regulation: 21 CFR 868.2377
Advisory panel: Anesthesiology
Date received: 1989-08-07
Decision date: 1989-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, D.C., DC, US

Download summary PDF View on FDA.gov ↗

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