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FDA 510(k)

STEREO COLLIMATOR RF-T SERIES

K-Number: K920733 · 1992-04-16

ApplicantShimadzu Medical Systems
Decision Date1992-04-16
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STEREO COLLIMATOR RF-T SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Medical Systems. It received FDA 510(k) clearance on 1992-04-16 under 510(k) number K920733. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEREO COLLIMATOR RF-T SERIES?

STEREO COLLIMATOR RF-T SERIES is a medical device that received FDA 510(k) clearance on 1992-04-16. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K920733.

When did STEREO COLLIMATOR RF-T SERIES receive FDA 510(k) clearance?

STEREO COLLIMATOR RF-T SERIES received FDA 510(k) clearance on 1992-04-16, under 510(k) number K920733.

Who is the listed applicant for STEREO COLLIMATOR RF-T SERIES?

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

What is the FDA product code for STEREO COLLIMATOR RF-T SERIES?

The FDA product code for STEREO COLLIMATOR RF-T SERIES is IZW.

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Other records listing Shimadzu Medical Systems 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.

K082224DIAGNOSTIC ULTRASOUND SYSTEM SARANO, ECHO VIEW, SHIMASONICK071291ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1100K071287ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PROK071289ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PROK061643ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PROK061637ECHOVIEW/ SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-2200PRO

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Related Devices (Code: IZW)

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.

K101039SHIMADZU COLLIMATOR R-300Shimadzu Corp.K093572R650 QDASM COLLIMATOROmega Medical Imaging, Inc.K090578SHIMADZU COLLIMATOR R-30HShimadzu Corp.K091517RALCO, MODEL R225 ACSRalco S.R.L.K083029MODEL R605DASM AUTOMATIC X-RAY COLLIMATORRalco S.R.L.K072780MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATORRalco S.R.L.

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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