APTA-BRONCHOSCREEN
K-Number: K843852 · 1984-11-01
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Device Summary
Frequently Asked Questions
What is the APTA-BRONCHOSCREEN?
APTA-BRONCHOSCREEN is a medical device that received FDA 510(k) clearance on 1984-11-01. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K843852.
When did APTA-BRONCHOSCREEN receive FDA 510(k) clearance?
APTA-BRONCHOSCREEN received FDA 510(k) clearance on 1984-11-01, under 510(k) number K843852.
Who is the listed applicant for APTA-BRONCHOSCREEN?
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 APTA-BRONCHOSCREEN?
The FDA product code for APTA-BRONCHOSCREEN is BZC.
Related Clinical Trials
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.
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.
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.
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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