BML SERIES
K-Number: K903529 · 1991-01-23
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Device Summary
Frequently Asked Questions
What is the BML SERIES?
BML SERIES is a medical device that received FDA 510(k) clearance on 1991-01-23. The listed applicant is Olympus Corp.. The 510(k) number is K903529.
When did BML SERIES receive FDA 510(k) clearance?
BML SERIES received FDA 510(k) clearance on 1991-01-23, under 510(k) number K903529.
Who is the listed applicant for BML SERIES?
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 BML SERIES?
The FDA product code for BML SERIES is LQC.
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: LQC)
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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