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FDA 510(k)

AUTOMATIC POSITIVE BEAM COLLIMATOR

K-Number: K791504 · 1979-09-07

ApplicantDial-X Instruments, Inc.
Decision Date1979-09-07
Product CodeKPW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC POSITIVE BEAM COLLIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dial-X Instruments, Inc.. It received FDA 510(k) clearance on 1979-09-07 under 510(k) number K791504. The device is classified under product code KPW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC POSITIVE BEAM COLLIMATOR?

AUTOMATIC POSITIVE BEAM COLLIMATOR is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Dial-X Instruments, Inc.. The 510(k) number is K791504.

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

AUTOMATIC POSITIVE BEAM COLLIMATOR received FDA 510(k) clearance on 1979-09-07, under 510(k) number K791504.

Who is the listed applicant for AUTOMATIC POSITIVE BEAM COLLIMATOR?

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

What is the FDA product code for AUTOMATIC POSITIVE BEAM COLLIMATOR?

The FDA product code for AUTOMATIC POSITIVE BEAM COLLIMATOR is KPW.

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Related Devices (Code: KPW)

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.

K093596LUMOS, MODEL R 72BLumos, Inc.K062788COLLIMATOR, MODEL M-38Umi InternationalK030487R 72Ralco S.R.L.K954310BLA-800AToshiba Medical SystemsK946320R 302Ralco S.R.L.K914184P2020-8-0 BEAM-LIMITING DEVICEPrecise Optics

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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