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FDA 510(k)

OHMEDA BIOX 3700 PULSE OXIMETER

K-Number: K850494 · 1985-03-28

ApplicantOhmeda Medical
Decision Date1985-03-28
Product CodeDPZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OHMEDA BIOX 3700 PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1985-03-28 under 510(k) number K850494. The device is classified under product code DPZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA BIOX 3700 PULSE OXIMETER?

OHMEDA BIOX 3700 PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1985-03-28. The listed applicant is Ohmeda Medical. The 510(k) number is K850494.

When did OHMEDA BIOX 3700 PULSE OXIMETER receive FDA 510(k) clearance?

OHMEDA BIOX 3700 PULSE OXIMETER received FDA 510(k) clearance on 1985-03-28, under 510(k) number K850494.

Who is the listed applicant for OHMEDA BIOX 3700 PULSE OXIMETER?

The FDA 510(k) record lists Ohmeda Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OHMEDA BIOX 3700 PULSE OXIMETER?

The FDA product code for OHMEDA BIOX 3700 PULSE OXIMETER is DPZ.

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Other records listing Ohmeda Medical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

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Related Devices (Code: DPZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K042675FLEXI-STAT SP02 EAR SENSORElekon Industries U.S.A., Inc.K040831DATEX-OHMEDA TRUSAT PULSE OXIMETER AND ACCESSORIES, MODEL 3500Datex-Ohmeda, Inc.K012333FLEXI-SITE SP02 EAR SENSOREpic Medical Equipment Services, Inc.K010718FLEXI-SITE SP02 EAR SENSOREpic Medical Equipment Services, Inc.K944760DURA-Y OXYGEN TRANSDUCER, EAR CLIPNellcor, Inc.K942752MARQUETTE EAR PROBE SENSORMarquette Electronics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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