OHMEDA TEC 6 CONTINUOUS FLOW VAPORIZER— 510(k) K913593

Name: FDA 510(k) clearance K913593
Creator: U.S. Food and Drug Administration
Published: 1992-10-06

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K913593 for OHMEDA TEC 6 CONTINUOUS FLOW VAPORIZER, Substantially Equivalent on 1992-10-06. Applicant: Ohmeda Medical. Device class: 2.

Clearance details

Applicant: Ohmeda Medical
Product code: Code CAD
Device class: Class 2
Regulation: 21 CFR 868.5880
Advisory panel: Anesthesiology
Date received: 1991-08-13
Decision date: 1992-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAD

view all

K240375 — V80 Anesthetic Vaporizer (V80)2024-10-31
K172702 — Tec 820, Tec 8502018-01-04
K150167 — V60 Anesthetic Vaporizer2015-06-30
K110608 — SEVOFLURANE VAPORIZER ADAPTOR2011-07-20
K060331 — SIGMA ALPHA VAPORIZER2006-05-10

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

Adverse events under product code CAD

product code CAD

Malfunction: 3,275
Total: 3,275

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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