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FDA 510(k)

AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO

K-Number: K001502 · 2000-07-12

ApplicantErich Jaeger GmbH
Decision Date2000-07-12
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger GmbH. It received FDA 510(k) clearance on 2000-07-12 under 510(k) number K001502. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO?

AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO is a medical device that received FDA 510(k) clearance on 2000-07-12. The listed applicant is Erich Jaeger GmbH. The 510(k) number is K001502.

When did AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO receive FDA 510(k) clearance?

AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO received FDA 510(k) clearance on 2000-07-12, under 510(k) number K001502.

Who is the listed applicant for AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO?

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

What is the FDA product code for AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO?

The FDA product code for AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO is BZC.

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Other records listing Erich Jaeger GmbH 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.

K023120OXYCON MOBILEK023796MS PAED-BABY BODYK021138SLEEPSCREEN/APNOESCREEN CARDIOK000648SPIRO PRO

Related Devices (Code: BZC)

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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