BRONCHOSCOPE BF-N20
K-Number: K910423 · 1991-04-29
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Device Summary
Frequently Asked Questions
What is the BRONCHOSCOPE BF-N20?
BRONCHOSCOPE BF-N20 is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is Olympus Corp.. The 510(k) number is K910423.
When did BRONCHOSCOPE BF-N20 receive FDA 510(k) clearance?
BRONCHOSCOPE BF-N20 received FDA 510(k) clearance on 1991-04-29, under 510(k) number K910423.
Who is the listed applicant for BRONCHOSCOPE BF-N20?
The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRONCHOSCOPE BF-N20?
The FDA product code for BRONCHOSCOPE BF-N20 is EOQ.
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 Olympus Corp. 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: EOQ)
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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