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FDA 510(k)

DIGITAL RADIOGRAPHY EXAMINATION TABLE

K-Number: K828313 · 1982-10-07

ApplicantEngineering Dynamics Corp.
Decision Date1982-10-07
Product Code
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY EXAMINATION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Engineering Dynamics Corp.. It received FDA 510(k) clearance on 1982-10-07 under 510(k) number K828313. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL RADIOGRAPHY EXAMINATION TABLE?

DIGITAL RADIOGRAPHY EXAMINATION TABLE is a medical device that received FDA 510(k) clearance on 1982-10-07. The listed applicant is Engineering Dynamics Corp.. The 510(k) number is K828313.

When did DIGITAL RADIOGRAPHY EXAMINATION TABLE receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY EXAMINATION TABLE received FDA 510(k) clearance on 1982-10-07, under 510(k) number K828313.

Who is the listed applicant for DIGITAL RADIOGRAPHY EXAMINATION TABLE?

The FDA 510(k) record lists Engineering Dynamics Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Engineering Dynamics Corp. 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.

K871494UPPERCYCLE STATIONARY EXERCISE MACHINESK844578NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONAK842108UNIVERSAL EXAMINATION TABLEK834098STATIONARY EXERCISE BICYCLEK802254GENERAL ULTRASOUND EXAM. TABLEK790545STRESS TESTING SYSTEM, LATERAL TILTING

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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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