OHMEDA 5500 AIRWAY PRESSURE MONITOR— 510(k) K864536

Name: FDA 510(k) clearance K864536
Creator: U.S. Food and Drug Administration
Published: 1987-01-12

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K864536 for OHMEDA 5500 AIRWAY PRESSURE MONITOR, Substantially Equivalent on 1987-01-12. Applicant: Ohmeda Medical. Device class: 2.

Clearance details

Applicant: Ohmeda Medical
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1986-11-17
Decision date: 1987-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAP

view all

K201666 — SINGLE USE MANOMETER2020-11-13
K182292 — VORTRAN APM-Plus2019-09-18
K180510 — NS 120P-TRS Airway Pressure Gauge2019-05-01
K172284 — NAPA LP-15 Airway Pressure Monitor2018-02-09
K153733 — VORTRAN Manometer2016-09-16

More clearances from Ohmeda Medical

view all

K123309 — GIRAFFE AND PANDA WARMERS2013-02-05
K101778 — GIRAFFE INCUBATOR2010-07-21
K101788 — GIRAFFE OMNIBED2010-07-21
K090697 — MODIFICATION TO: GIRAFFE AND PANDA WARMER2009-04-16
K072157 — MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)2007-08-27

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