TEK-PRO TEK-TATOR V ROTATOR & HUMIDIFY— 510(k) K820043

Name: FDA 510(k) clearance K820043
Creator: U.S. Food and Drug Administration
Published: 1982-01-28

Substantially Equivalent

American Dade

FDA 510(k) clearance K820043 for TEK-PRO TEK-TATOR V ROTATOR & HUMIDIFY, Substantially Equivalent on 1982-01-28. Applicant: American Dade. Device class: 1.

Clearance details

Applicant: American Dade
Product code: Code LIB
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1982-01-07
Decision date: 1982-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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