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FDA 510(k)

DIAL X COLLIMATOR MODEL A&B

K-Number: K771689 · 1977-09-14

ApplicantBennett X-Ray Corp.
Decision Date1977-09-14
Product CodeIZX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAL X COLLIMATOR MODEL A&B 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 1977-09-14 under 510(k) number K771689. The device is classified under product code IZX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAL X COLLIMATOR MODEL A&B?

DIAL X COLLIMATOR MODEL A&B is a medical device that received FDA 510(k) clearance on 1977-09-14. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K771689.

When did DIAL X COLLIMATOR MODEL A&B receive FDA 510(k) clearance?

DIAL X COLLIMATOR MODEL A&B received FDA 510(k) clearance on 1977-09-14, under 510(k) number K771689.

Who is the listed applicant for DIAL X COLLIMATOR MODEL A&B?

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 DIAL X COLLIMATOR MODEL A&B?

The FDA product code for DIAL X COLLIMATOR MODEL A&B is IZX.

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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

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Related Devices (Code: IZX)

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.

K110856RALCORalco S.R.L.K101036SHIMADZU COLLIMATOR R-20JShimadzu Corp.K042840SHIMADZU COLLIMATOR R-20JShimadzu Corp.K031771SHIMADZU COLLIMATOR R-30HShimadzu Corp.K981267FACTS MONOBLOCKDynarad Corp.K974240LIGHTLINE-MWuestec Medical, 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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