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FDA 510(k)

ARVEE APNEA MONITOR, MODEL 2400

K-Number: K891676 · 1989-09-06

ApplicantArvee Medical, Inc.
Decision Date1989-09-06
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARVEE APNEA MONITOR, MODEL 2400 is the device name listed in this FDA 510(k) record. The listed applicant is Arvee Medical, Inc.. It received FDA 510(k) clearance on 1989-09-06 under 510(k) number K891676. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARVEE APNEA MONITOR, MODEL 2400?

ARVEE APNEA MONITOR, MODEL 2400 is a medical device that received FDA 510(k) clearance on 1989-09-06. The listed applicant is Arvee Medical, Inc.. The 510(k) number is K891676.

When did ARVEE APNEA MONITOR, MODEL 2400 receive FDA 510(k) clearance?

ARVEE APNEA MONITOR, MODEL 2400 received FDA 510(k) clearance on 1989-09-06, under 510(k) number K891676.

Who is the listed applicant for ARVEE APNEA MONITOR, MODEL 2400?

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

What is the FDA product code for ARVEE APNEA MONITOR, MODEL 2400?

The FDA product code for ARVEE APNEA MONITOR, MODEL 2400 is BZQ.

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 Arvee Medical, Inc. 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.

K900730ARVEE APNEA MONITOR, MODEL 4800K872631INFANT MONITOR, MODEL 2400

Related Devices (Code: BZQ)

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

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

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