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FDA 510(k)

RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC

K-Number: K820306 · 1982-03-05

ApplicantTecnomed, Inc.
Decision Date1982-03-05
Product CodeKPW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC is the device name listed in this FDA 510(k) record. The listed applicant is Tecnomed, Inc.. It received FDA 510(k) clearance on 1982-03-05 under 510(k) number K820306. 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 RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC?

RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC is a medical device that received FDA 510(k) clearance on 1982-03-05. The listed applicant is Tecnomed, Inc.. The 510(k) number is K820306.

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

RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC received FDA 510(k) clearance on 1982-03-05, under 510(k) number K820306.

Who is the listed applicant for RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC?

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

What is the FDA product code for RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC?

The FDA product code for RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC is KPW.

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Other records listing Tecnomed, Inc. 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.

K892226TEC 6340 90/15 RADIOGRAPHIC/FLUOROSCOPIC TABLEK854203TEC 2720 MAMEX DC MAGK820307TECNOMED GENERATOR, RADIOGRAPH., 3 PHASEK827126TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASEK827124RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHICK820305RALCO COLLIMATORS, MANUAL RADIOGRAPHIC

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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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