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FDA 510(k)

TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR

K-Number: K860203 · 1986-01-30

Decision Date1986-01-30
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Tingle X-Ray Products, Inc.. It received FDA 510(k) clearance on 1986-01-30 under 510(k) number K860203. 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 TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR?

TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Tingle X-Ray Products, Inc.. The 510(k) number is K860203.

When did TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR receive FDA 510(k) clearance?

TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR received FDA 510(k) clearance on 1986-01-30, under 510(k) number K860203.

Who is the listed applicant for TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR?

The FDA 510(k) record lists Tingle X-Ray Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR?

The FDA product code for TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR 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 Tingle X-Ray Products, 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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