I.V. SENTINEL— 510(k) K821823

Substantially Equivalent

The John Bunn Co.

FDA 510(k) clearance K821823 for I.V. SENTINEL, Substantially Equivalent on 1982-08-16. Applicant: The John Bunn Co.. Device class: 2.

Clearance details

Applicant: The John Bunn Co.
Product code: Code FLN
Device class: Class 2
Regulation: 21 CFR 880.2420
Advisory panel: General Hospital
Date received: 1982-06-22
Decision date: 1982-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from The John Bunn Co.

K900854 — JOHN BUNN: MEDIX COMPACT TRAVELLER1990-04-23
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K873071 — BUNN CONCENTRATOR MODEL 2100 SERIES1987-09-15
K870094 — BUNN MODEL 530 ASPIRATOR1987-03-06
K861435 — BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVE1986-11-07

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