CARHILL ONE-WAY RESUSCITATION VALVE— 510(k) K864681

Name: FDA 510(k) clearance K864681
Creator: U.S. Food and Drug Administration
Published: 1987-05-21

Substantially Equivalent

Life Design Systems, Inc.

FDA 510(k) clearance K864681 for CARHILL ONE-WAY RESUSCITATION VALVE, Substantially Equivalent on 1987-05-21. Applicant: Life Design Systems, Inc.. Device class: 2.

Clearance details

Applicant: Life Design Systems, Inc.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1986-12-02
Decision date: 1987-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CBP

view all

K241366 — QualityFlow O2 Series (QualityFLOW O2); QualityFlow O2 Series (QualityFLOW O2 MTV)2024-10-29
K234053 — F&P Optiflow Flow Diverter2024-08-09
K210992 — Altech® Exhalation Valve (Single Limb and Dual Limb)2021-12-23
K192285 — CPR Face Shield2020-11-25
K173770 — OJR215 Pressure Relief Manifold2019-04-05

More clearances from Life Design Systems, Inc.

view all

K913714 — MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)1992-12-01
K885313 — HUMIDI-FLEX TM1989-10-11
K893030 — CHILD SIZE - FILTER FLEX (TM)1989-09-18
K892862 — FLEX-CUP PERCUSSOR1989-05-25
K892221 — PULMONARY RESUSCITATOR, MODIFICATION1989-05-18

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