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FDA 510(k)

ASTHMA MONITOR

K-Number: K960078 · 1996-09-20

ApplicantErich Jaeger, Inc.
Decision Date1996-09-20
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ASTHMA MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger, Inc.. It received FDA 510(k) clearance on 1996-09-20 under 510(k) number K960078. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTHMA MONITOR?

ASTHMA MONITOR is a medical device that received FDA 510(k) clearance on 1996-09-20. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K960078.

When did ASTHMA MONITOR receive FDA 510(k) clearance?

ASTHMA MONITOR received FDA 510(k) clearance on 1996-09-20, under 510(k) number K960078.

Who is the listed applicant for ASTHMA MONITOR?

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

What is the FDA product code for ASTHMA MONITOR?

The FDA product code for ASTHMA MONITOR is BZG.

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Related Devices (Code: BZG)

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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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