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FDA 510(k)

BIRD MONITOR INTERFACE

K-Number: K982580 · 1998-10-22

ApplicantBird Products Corp.
Decision Date1998-10-22
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

BIRD MONITOR INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Bird Products Corp.. It received FDA 510(k) clearance on 1998-10-22 under 510(k) number K982580. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the BIRD MONITOR INTERFACE?

BIRD MONITOR INTERFACE is a medical device that received FDA 510(k) clearance on 1998-10-22. The listed applicant is Bird Products Corp.. The 510(k) number is K982580.

When did BIRD MONITOR INTERFACE receive FDA 510(k) clearance?

BIRD MONITOR INTERFACE received FDA 510(k) clearance on 1998-10-22, under 510(k) number K982580.

Who is the listed applicant for BIRD MONITOR INTERFACE?

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

What is the FDA product code for BIRD MONITOR INTERFACE?

The FDA product code for BIRD MONITOR INTERFACE is CBK.

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Other records listing Bird Products Corp. 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.

K032451BIRD TBIRD VELA VENTILATORK022674BIRD AVEA VENTILATORK020730ORION NASAL CPAP SYSTEMK013642AVEAK020746BIRD TBIRD VELA VENTILATORK003770BIRD TBIRD LEGACY VENTILATOR

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Related Devices (Code: CBK)

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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