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FDA 510(k)

AUTO-TECH GENERATOR

K-Number: K827662 · 1982-08-16

ApplicantBennett X-Ray Corp.
Decision Date1982-08-16
Product Code
DecisionSubstantially Equivalent

Device Summary

AUTO-TECH GENERATOR 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 1982-08-16 under 510(k) number K827662. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-TECH GENERATOR?

AUTO-TECH GENERATOR is a medical device that received FDA 510(k) clearance on 1982-08-16. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K827662.

When did AUTO-TECH GENERATOR receive FDA 510(k) clearance?

AUTO-TECH GENERATOR received FDA 510(k) clearance on 1982-08-16, under 510(k) number K827662.

Who is the listed applicant for AUTO-TECH GENERATOR?

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

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.

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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 →

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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