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FDA 510(k)

TED 200T7 OXYGEN MONITOR

K-Number: K990403 · 2000-02-03

ApplicantTeledyne Electronic Technologies
Decision Date2000-02-03
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TED 200T7 OXYGEN MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Electronic Technologies. It received FDA 510(k) clearance on 2000-02-03 under 510(k) number K990403. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TED 200T7 OXYGEN MONITOR?

TED 200T7 OXYGEN MONITOR is a medical device that received FDA 510(k) clearance on 2000-02-03. The listed applicant is Teledyne Electronic Technologies. The 510(k) number is K990403.

When did TED 200T7 OXYGEN MONITOR receive FDA 510(k) clearance?

TED 200T7 OXYGEN MONITOR received FDA 510(k) clearance on 2000-02-03, under 510(k) number K990403.

Who is the listed applicant for TED 200T7 OXYGEN MONITOR?

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

What is the FDA product code for TED 200T7 OXYGEN MONITOR?

The FDA product code for TED 200T7 OXYGEN MONITOR is CCL.

Related Clinical Trials

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.

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Other records listing Teledyne Electronic Technologies 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.

K990457TED 60T OXYGEN ANALYZER

Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, 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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