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FDA 510(k)

260 CORVUS

K-Number: K003292 · 2001-01-05

ApplicantPie Medical
Decision Date2001-01-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

260 CORVUS is the device name listed in this FDA 510(k) record. The listed applicant is Pie Medical. It received FDA 510(k) clearance on 2001-01-05 under 510(k) number K003292. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 260 CORVUS?

260 CORVUS is a medical device that received FDA 510(k) clearance on 2001-01-05. The listed applicant is Pie Medical. The 510(k) number is K003292.

When did 260 CORVUS receive FDA 510(k) clearance?

260 CORVUS received FDA 510(k) clearance on 2001-01-05, under 510(k) number K003292.

Who is the listed applicant for 260 CORVUS?

The FDA 510(k) record lists Pie Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 260 CORVUS?

The FDA product code for 260 CORVUS is IYO.

Related Clinical Trials

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Other records listing Pie Medical 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.

K061961ART LAB SOFTWAREK053154MYLAB15/20 3D/4D ULTRASOUND IMAGING SYSTEMK043588MYLAB 15 / MYLAB 20, MODEL 2700K043360IMT.LABK041675PICUS, PARUS, FALCO AND AQUILA ULTRASOUND SYSTEMSK033604TRINGA ULTRASOUND IMAGING SYSTEM, MODEL 50L

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Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.

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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