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FDA 510(k)

HFQ SERIES CONTROLS AND GENERATORS

K-Number: K905799 · 1991-02-26

ApplicantBennett X-Ray Corp.
Decision Date1991-02-26
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HFQ SERIES CONTROLS AND GENERATORS 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 1991-02-26 under 510(k) number K905799. 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 HFQ SERIES CONTROLS AND GENERATORS?

HFQ SERIES CONTROLS AND GENERATORS is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K905799.

When did HFQ SERIES CONTROLS AND GENERATORS receive FDA 510(k) clearance?

HFQ SERIES CONTROLS AND GENERATORS received FDA 510(k) clearance on 1991-02-26, under 510(k) number K905799.

Who is the listed applicant for HFQ SERIES CONTROLS AND GENERATORS?

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 HFQ SERIES CONTROLS AND GENERATORS?

The FDA product code for HFQ SERIES CONTROLS AND GENERATORS is IZO.

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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.

K964576PROFILE MAMMOGRAPHY SYSTEM (M-PRO)K952672VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEMK944978BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSIK945962BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHYK945731HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORSK945749BENNETT X-RAY TOMOGRAPHY SYSTEM

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, Inc.

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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