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FDA 510(k)

ERGO-PNEUMOTEST

K-Number: K853434 · 1986-02-05

ApplicantErich Jaeger, Inc.
Decision Date1986-02-05
Product CodeBZL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ERGO-PNEUMOTEST 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 1986-02-05 under 510(k) number K853434. The device is classified under product code BZL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERGO-PNEUMOTEST?

ERGO-PNEUMOTEST is a medical device that received FDA 510(k) clearance on 1986-02-05. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K853434.

When did ERGO-PNEUMOTEST receive FDA 510(k) clearance?

ERGO-PNEUMOTEST received FDA 510(k) clearance on 1986-02-05, under 510(k) number K853434.

Who is the listed applicant for ERGO-PNEUMOTEST?

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 ERGO-PNEUMOTEST?

The FDA product code for ERGO-PNEUMOTEST is BZL.

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Other records listing Erich Jaeger, 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.

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Related Devices (Code: BZL)

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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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