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FDA 510(k)

BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR

K-Number: K892841 · 1989-10-05

ApplicantBedfont Technical Instruments , Ltd.
Decision Date1989-10-05
Product CodeCCJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Bedfont Technical Instruments , Ltd.. It received FDA 510(k) clearance on 1989-10-05 under 510(k) number K892841. The device is classified under product code CCJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR?

BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR is a medical device that received FDA 510(k) clearance on 1989-10-05. The listed applicant is Bedfont Technical Instruments , Ltd.. The 510(k) number is K892841.

When did BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR receive FDA 510(k) clearance?

BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR received FDA 510(k) clearance on 1989-10-05, under 510(k) number K892841.

Who is the listed applicant for BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR?

The FDA 510(k) record lists Bedfont Technical Instruments , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR?

The FDA product code for BEDFONT EC50 SMOKERLYZER CARBON MONOXIDE MONITOR is CCJ.

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Related Devices (Code: CCJ)

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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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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