ATI DISP. BIOLOGICAL TEST PACK FOR ETHYLENE OXIDE— 510(k) K895704

Name: FDA 510(k) clearance K895704
Creator: U.S. Food and Drug Administration
Published: 1990-03-08

Substantially Equivalent

Pymah Corp., Ati Div.

FDA 510(k) clearance K895704 for ATI DISP. BIOLOGICAL TEST PACK FOR ETHYLENE OXIDE, Substantially Equivalent on 1990-03-08. Applicant: Pymah Corp., Ati Div.. Device class: 2.

Clearance details

Applicant: Pymah Corp., Ati Div.
Product code: Code FRC
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1989-09-22
Decision date: 1990-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Potomac, MD, US

Download summary PDF View on FDA.gov ↗

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