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FDA 510(k)

RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHIC

K-Number: K827124 · 1982-03-05

ApplicantTecnomed, Inc.
Decision Date1982-03-05
Product Code
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 K827124. 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 K827124.

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 K827124.

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.

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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 PHASEK820306RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHICK820305RALCO COLLIMATORS, MANUAL RADIOGRAPHIC

View all 18 devices →

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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