OHMEDA BIOX 3700 PULSE OXIMETER— 510(k) K850494

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K850494 for OHMEDA BIOX 3700 PULSE OXIMETER, Substantially Equivalent on 1985-03-28. Applicant: Ohmeda Medical. Device class: 2.

Clearance details

Applicant: Ohmeda Medical
Product code: Code DPZ
Device class: Class 2
Regulation: 21 CFR 870.2710
Advisory panel: Cardiovascular
Date received: 1985-02-08
Decision date: 1985-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DPZ

K042675 — FLEXI-STAT SP02 EAR SENSOR2004-12-06
K040831 — DATEX-OHMEDA TRUSAT PULSE OXIMETER AND ACCESSORIES, MODEL 35002004-09-02
K012333 — FLEXI-SITE SP02 EAR SENSOR2001-10-17
K010718 — FLEXI-SITE SP02 EAR SENSOR2001-03-23
K944760 — DURA-Y OXYGEN TRANSDUCER, EAR CLIP1994-10-17

More clearances from Ohmeda Medical

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.