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FDA 510(k)

30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE

K-Number: K894479 · 1989-09-12

Decision Date1989-09-12
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1989-09-12 under 510(k) number K894479. 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 30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE?

30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE is a medical device that received FDA 510(k) clearance on 1989-09-12. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K894479.

When did 30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE receive FDA 510(k) clearance?

30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE received FDA 510(k) clearance on 1989-09-12, under 510(k) number K894479.

Who is the listed applicant for 30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE?

The FDA 510(k) record lists Bennett X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE?

The FDA product code for 30KW HIGH FREQ. RADIO. GENE. MODELS HFQ-30/HFQ30SE 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 Bennett X-Ray Corp. 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 23 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

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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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