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FDA 510(k)

LIGHT BEAM COLLIMATOR

K-Number: K843244 · 1984-09-14

ApplicantDealers X-Ray Co., Inc.
Decision Date1984-09-14
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIGHT BEAM COLLIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dealers X-Ray Co., Inc.. It received FDA 510(k) clearance on 1984-09-14 under 510(k) number K843244. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT BEAM COLLIMATOR?

LIGHT BEAM COLLIMATOR is a medical device that received FDA 510(k) clearance on 1984-09-14. The listed applicant is Dealers X-Ray Co., Inc.. The 510(k) number is K843244.

When did LIGHT BEAM COLLIMATOR receive FDA 510(k) clearance?

LIGHT BEAM COLLIMATOR received FDA 510(k) clearance on 1984-09-14, under 510(k) number K843244.

Who is the listed applicant for LIGHT BEAM COLLIMATOR?

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

What is the FDA product code for LIGHT BEAM COLLIMATOR?

The FDA product code for LIGHT BEAM COLLIMATOR is IZW.

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Related Devices (Code: IZW)

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.

K101039SHIMADZU COLLIMATOR R-300Shimadzu Corp.K093572R650 QDASM COLLIMATOROmega Medical Imaging, Inc.K090578SHIMADZU COLLIMATOR R-30HShimadzu Corp.K091517RALCO, MODEL R225 ACSRalco S.R.L.K083029MODEL R605DASM AUTOMATIC X-RAY COLLIMATORRalco S.R.L.K072780MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATORRalco S.R.L.

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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