OLYMPUS ANGIOSCOPY PUMP
K-Number: K871422 · 1987-08-12
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Device Summary
Frequently Asked Questions
What is the OLYMPUS ANGIOSCOPY PUMP?
OLYMPUS ANGIOSCOPY PUMP is a medical device that received FDA 510(k) clearance on 1987-08-12. The listed applicant is Olympus Corp.. The 510(k) number is K871422.
When did OLYMPUS ANGIOSCOPY PUMP receive FDA 510(k) clearance?
OLYMPUS ANGIOSCOPY PUMP received FDA 510(k) clearance on 1987-08-12, under 510(k) number K871422.
Who is the listed applicant for OLYMPUS ANGIOSCOPY PUMP?
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 OLYMPUS ANGIOSCOPY PUMP?
The FDA product code for OLYMPUS ANGIOSCOPY PUMP is DQI.
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: DQI)
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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