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FDA 510(k)

OLYMPUS BF TYPE UM40

K-Number: K021204 · 2002-05-01

ApplicantOlympus Optical Co., Ltd.
Decision Date2002-05-01
Product CodePSV
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OLYMPUS BF TYPE UM40 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Optical Co., Ltd.. It received FDA 510(k) clearance on 2002-05-01 under 510(k) number K021204. The device is classified under product code PSV. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS BF TYPE UM40?

OLYMPUS BF TYPE UM40 is a medical device that received FDA 510(k) clearance on 2002-05-01. The listed applicant is Olympus Optical Co., Ltd.. The 510(k) number is K021204.

When did OLYMPUS BF TYPE UM40 receive FDA 510(k) clearance?

OLYMPUS BF TYPE UM40 received FDA 510(k) clearance on 2002-05-01, under 510(k) number K021204.

Who is the listed applicant for OLYMPUS BF TYPE UM40?

The FDA 510(k) record lists Olympus Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS BF TYPE UM40?

The FDA product code for OLYMPUS BF TYPE UM40 is PSV.

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Other records listing Olympus Optical Co., Ltd. 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.

K033225EVIS EXERA BRONCHOFIBERVIDEOSCOPE OLYMPUS BF TYPE XP160F, ITS ACCESSORIES AND ANCILLARY EQUIPMENTK031305OLYMPUS ULTRASONIC SURGICAL SYSTEMK031648VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE VK032092OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPEK031347ULTRASONIC GASTROVIDEOSCOPE, TYPE UC160P-AT8 AND UCT160-AT8K024138HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE

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Related Devices (Code: PSV)

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.

K260401EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE OLYMPUS BF-UCP190F (BF-UCP190F)Olympus Medical Systems CorporationK183525EVIS EUS Ultrasound Bronchofibervideoscope Olympus BF-UC190FOlympus Medical Systems Corp.K070983OLYMPUS XBF-UC180F-DT8 ULTRASONIC BRONCHOFIBERVIDEOSCOPE USED WITH ALOKA SSD-ALPHA 5/10 ULTRASOUND SYSTEMOlympus Medical Systems Corporation

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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