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FDA 510(k)

TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE

K-Number: K827126 · 1982-03-05

ApplicantTecnomed, Inc.
Decision Date1982-03-05
Product Code
DecisionSubstantially Equivalent

Device Summary

TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE 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 K827126. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE?

TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE 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 K827126.

When did TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE receive FDA 510(k) clearance?

TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE received FDA 510(k) clearance on 1982-03-05, under 510(k) number K827126.

Who is the listed applicant for TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE?

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 RADIOGRAPHICK820305RALCO COLLIMATORS, MANUAL RADIOGRAPHIC

View all 18 devices →

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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