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FDA 510(k)

SHIMADZU CEILING-SUSPENDED C-ARM CH-50

K-Number: K875374 · 1988-02-12

ApplicantShimadzu Precision Instruments, Inc.
Decision Date1988-02-12
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU CEILING-SUSPENDED C-ARM CH-50 is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Precision Instruments, Inc.. It received FDA 510(k) clearance on 1988-02-12 under 510(k) number K875374. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHIMADZU CEILING-SUSPENDED C-ARM CH-50?

SHIMADZU CEILING-SUSPENDED C-ARM CH-50 is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is Shimadzu Precision Instruments, Inc.. The 510(k) number is K875374.

When did SHIMADZU CEILING-SUSPENDED C-ARM CH-50 receive FDA 510(k) clearance?

SHIMADZU CEILING-SUSPENDED C-ARM CH-50 received FDA 510(k) clearance on 1988-02-12, under 510(k) number K875374.

Who is the listed applicant for SHIMADZU CEILING-SUSPENDED C-ARM CH-50?

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

What is the FDA product code for SHIMADZU CEILING-SUSPENDED C-ARM CH-50?

The FDA product code for SHIMADZU CEILING-SUSPENDED C-ARM CH-50 is IZI.

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Other records listing Shimadzu Precision Instruments, Inc. 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.

K940294SHIMADZU MOBILE X-RAY SYSTEMSK890913SDU 800 DIAGNOSTIC ULTRASOUND INSTRUMENTK884598SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200K884477SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150BK875378SINGLE PHOTON SET 031 & AZ-701-NTS-SP EMISSIONK882311SHIMADZU LATERAL C-ARM MH-31

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Related Devices (Code: IZI)

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.

K261037780 nm SPY Portable Handheld Imaging (SPY-PHI) SystemStryker EndoscopyK253181SURGIMAGE SIM 1000H Fluorescence Imaging PlatformSurgimage CorporationK243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbHK243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision 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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