LOW PRESSURE ALARM FOR OXYGEN CYLINDER— 510(k) K843212

Name: FDA 510(k) clearance K843212
Creator: U.S. Food and Drug Administration
Published: 1984-09-19

Substantially Equivalent

Hospitak, Inc.

FDA 510(k) clearance K843212 for LOW PRESSURE ALARM FOR OXYGEN CYLINDER, Substantially Equivalent on 1984-09-19. Applicant: Hospitak, Inc.. Device class: 1.

Clearance details

Applicant: Hospitak, Inc.
Product code: Code BXH
Device class: Class 1
Regulation: 21 CFR 868.2610
Advisory panel: Anesthesiology
Date received: 1984-08-15
Decision date: 1984-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXH

view all

K942645 — B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG1994-07-27
K853040 — PRESSURE GAUGE1985-10-10
K770614 — MONITOR, GAS MANIFOLD1977-04-07

More clearances from Hospitak, Inc.

view all

K955483 — TRACH MASK MODEL (245, 246)1996-02-28
K954787 — ILLUMINATOR1996-01-31
K953619 — WARM N WET HME W/LUER ADAPTER1995-08-25
K953620 — WARM N WET HMEF W/LUER ADAPTER1995-08-25
K915750 — DISPOSABLE BACTERIAL BREATHNG FILTER1994-11-30

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