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FDA 510(k)

SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES

K-Number: K933472 · 1994-02-07

ApplicantShimadzu Corp.
Decision Date1994-02-07
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K933472. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES?

SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Shimadzu Corp.. The 510(k) number is K933472.

When did SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES receive FDA 510(k) clearance?

SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES received FDA 510(k) clearance on 1994-02-07, under 510(k) number K933472.

Who is the listed applicant for SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES?

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

What is the FDA product code for SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES?

The FDA product code for SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES is JAA.

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Other records listing Shimadzu Corp. as applicant

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K101039SHIMADZU COLLIMATOR R-300K101036SHIMADZU COLLIMATOR R-20JK090578SHIMADZU COLLIMATOR R-30HK090268SHIMADZU MOBILE X-RAY SYSTEM MOBILE ART EVOLUTIONK080701SHIMADZU MOBILE X-RAY SYSTEM MOBILEDART EVOLUTIONK072006DAR-9400F

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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