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FDA 510(k)

STORZ COMPUSCAN AB

K-Number: K930278 · 1994-02-09

ApplicantStorz
Decision Date1994-02-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STORZ COMPUSCAN AB is the device name listed in this FDA 510(k) record. The listed applicant is Storz. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K930278. 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 STORZ COMPUSCAN AB?

STORZ COMPUSCAN AB is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Storz. The 510(k) number is K930278.

When did STORZ COMPUSCAN AB receive FDA 510(k) clearance?

STORZ COMPUSCAN AB received FDA 510(k) clearance on 1994-02-09, under 510(k) number K930278.

Who is the listed applicant for STORZ COMPUSCAN AB?

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

What is the FDA product code for STORZ COMPUSCAN AB?

The FDA product code for STORZ COMPUSCAN AB is IYO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Storz 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.

K960007STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATORK952151STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)K954340STORZ MICROFLOW PHACOEMULSIFICATION NEEDLEK926512STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVEK913504STORZ MICRO CUTTER 25 GAUGE PACK

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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