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FDA 510(k)

COLLIMATOR, AUTOMATIC

K-Number: K770335 · 1977-02-28

ApplicantLitton Medical Systems
Decision Date1977-02-28
Product CodeKPW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMATOR, AUTOMATIC is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Systems. It received FDA 510(k) clearance on 1977-02-28 under 510(k) number K770335. 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 COLLIMATOR, AUTOMATIC?

COLLIMATOR, AUTOMATIC is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Litton Medical Systems. The 510(k) number is K770335.

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

COLLIMATOR, AUTOMATIC received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770335.

Who is the listed applicant for COLLIMATOR, AUTOMATIC?

The FDA 510(k) record lists Litton Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLLIMATOR, AUTOMATIC?

The FDA product code for COLLIMATOR, AUTOMATIC is KPW.

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Other records listing Litton Medical Systems 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.

K770334TILTING X-RAY TABLEK770337FLUOROSCOPIC ASSEMBLY, IMAGE INTENS.K770333FLUOROSCOPE, C-ARMK770336X-RAY TUBE, ROTATING ANODEK770338X-RAY CONTROL & X-RAY HV GENERATORK760569THREE PHASE X-RAY CONTROLS & HV GENERATORS

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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

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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