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FDA 510(k)

INFANT MONITOR, MODEL 2400

K-Number: K872631 · 1987-10-26

ApplicantArvee Medical, Inc.
Decision Date1987-10-26
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INFANT 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 1987-10-26 under 510(k) number K872631. 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 INFANT MONITOR, MODEL 2400?

INFANT MONITOR, MODEL 2400 is a medical device that received FDA 510(k) clearance on 1987-10-26. The listed applicant is Arvee Medical, Inc.. The 510(k) number is K872631.

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

INFANT MONITOR, MODEL 2400 received FDA 510(k) clearance on 1987-10-26, under 510(k) number K872631.

Who is the listed applicant for INFANT 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 INFANT MONITOR, MODEL 2400?

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

Related Clinical Trials

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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 4800K891676ARVEE APNEA 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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