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FDA 510(k)

RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC

K-Number: K827125 · 1982-03-04

ApplicantTecnomed, Inc.
Decision Date1982-03-04
Product Code
DecisionSubstantially Equivalent

Device Summary

RALCO COLLIMATORS, MANUAL, 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 1982-03-04 under 510(k) number K827125. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC?

RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC is a medical device that received FDA 510(k) clearance on 1982-03-04. The listed applicant is Tecnomed, Inc.. The 510(k) number is K827125.

When did RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC receive FDA 510(k) clearance?

RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC received FDA 510(k) clearance on 1982-03-04, under 510(k) number K827125.

Who is the listed applicant for RALCO COLLIMATORS, MANUAL, 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 PHASEK827124RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHICK820306RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHICK827126TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE

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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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