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FDA 510(k)

CINESCAN S

K-Number: K021683 · 2002-06-21

ApplicantQuantel Medical
Decision Date2002-06-21
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CINESCAN S is the device name listed in this FDA 510(k) record. The listed applicant is Quantel Medical. It received FDA 510(k) clearance on 2002-06-21 under 510(k) number K021683. 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 CINESCAN S?

CINESCAN S is a medical device that received FDA 510(k) clearance on 2002-06-21. The listed applicant is Quantel Medical. The 510(k) number is K021683.

When did CINESCAN S receive FDA 510(k) clearance?

CINESCAN S received FDA 510(k) clearance on 2002-06-21, under 510(k) number K021683.

Who is the listed applicant for CINESCAN S?

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

What is the FDA product code for CINESCAN S?

The FDA product code for CINESCAN S is IYO.

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Other records listing Quantel Medical as applicant

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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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