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FDA 510(k)

X-RAY HIGH VOLTAGE GENERATOR ED 125L

K-Number: K920730 · 1992-04-27

Decision Date1992-04-27
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY HIGH VOLTAGE GENERATOR ED 125L 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 K920730. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY HIGH VOLTAGE GENERATOR ED 125L?

X-RAY HIGH VOLTAGE GENERATOR ED 125L 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 K920730.

When did X-RAY HIGH VOLTAGE GENERATOR ED 125L receive FDA 510(k) clearance?

X-RAY HIGH VOLTAGE GENERATOR ED 125L received FDA 510(k) clearance on 1992-04-27, under 510(k) number K920730.

Who is the listed applicant for X-RAY HIGH VOLTAGE GENERATOR ED 125L?

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 X-RAY HIGH VOLTAGE GENERATOR ED 125L?

The FDA product code for X-RAY HIGH VOLTAGE GENERATOR ED 125L is IZO.

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.

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.

View all 90 devices →

Related Devices (Code: IZO)

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.

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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