KENWOOD BIOLOGICAL STEOILIZ. INDICATOR— 510(k) K771132

Name: FDA 510(k) clearance K771132
Creator: U.S. Food and Drug Administration
Published: 1977-07-14

Substantially Equivalent

Will Ross Co.

FDA 510(k) clearance K771132 for KENWOOD BIOLOGICAL STEOILIZ. INDICATOR, Substantially Equivalent on 1977-07-14. Applicant: Will Ross Co.. Device class: 2.

Clearance details

Applicant: Will Ross Co.
Product code: Code FRC
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1977-06-23
Decision date: 1977-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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