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FDA 510(k)

OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE

K-Number: K871517 · 1987-11-30

ApplicantOlympus Corp.
Decision Date1987-11-30
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1987-11-30 under 510(k) number K871517. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE?

OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE is a medical device that received FDA 510(k) clearance on 1987-11-30. The listed applicant is Olympus Corp.. The 510(k) number is K871517.

When did OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE receive FDA 510(k) clearance?

OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE received FDA 510(k) clearance on 1987-11-30, under 510(k) number K871517.

Who is the listed applicant for OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE?

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 PF-25 ULTRATHIN ANGIOSCOPE?

The FDA product code for OLYMPUS PF-25 ULTRATHIN ANGIOSCOPE is DQX.

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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.

K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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Related Devices (Code: DQX)

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K253146Hyperdrive 35 GuidewireRapid-Medical , Ltd.K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd.K253667Accoat Guide WireSp Medical A/SK261640Merit MAK Nitinol/Gold-Tungsten Guide WireMerit Medical Ireland , Ltd.K254137InQwire Amplatz Guide WireMerit Medical Ireland, Ltd.K260544FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40FMD Co., Ltd.

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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