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FDA 510(k)

HIGH SPEED ROTATION STARTER SA-40

K-Number: K920723 · 1992-04-27

ApplicantShimadzu Medical Systems
Decision Date1992-04-27
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HIGH SPEED ROTATION STARTER SA-40 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 1992-04-27 under 510(k) number K920723. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH SPEED ROTATION STARTER SA-40?

HIGH SPEED ROTATION STARTER SA-40 is a medical device that received FDA 510(k) clearance on 1992-04-27. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K920723.

When did HIGH SPEED ROTATION STARTER SA-40 receive FDA 510(k) clearance?

HIGH SPEED ROTATION STARTER SA-40 received FDA 510(k) clearance on 1992-04-27, under 510(k) number K920723.

Who is the listed applicant for HIGH SPEED ROTATION STARTER SA-40?

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 HIGH SPEED ROTATION STARTER SA-40?

The FDA product code for HIGH SPEED ROTATION STARTER SA-40 is ITY.

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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: ITY)

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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.

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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