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FDA 510(k)

BREATHGUARD APNEA MONITOR

K-Number: K872833 · 1988-04-01

ApplicantLada Intl., Inc.
Decision Date1988-04-01
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BREATHGUARD APNEA MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Lada Intl., Inc.. It received FDA 510(k) clearance on 1988-04-01 under 510(k) number K872833. 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 BREATHGUARD APNEA MONITOR?

BREATHGUARD APNEA MONITOR is a medical device that received FDA 510(k) clearance on 1988-04-01. The listed applicant is Lada Intl., Inc.. The 510(k) number is K872833.

When did BREATHGUARD APNEA MONITOR receive FDA 510(k) clearance?

BREATHGUARD APNEA MONITOR received FDA 510(k) clearance on 1988-04-01, under 510(k) number K872833.

Who is the listed applicant for BREATHGUARD APNEA MONITOR?

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

What is the FDA product code for BREATHGUARD APNEA MONITOR?

The FDA product code for BREATHGUARD APNEA MONITOR is BZQ.

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Other records listing Lada Intl., Inc. as applicant

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Related Devices (Code: BZQ)

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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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