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FDA 510(k)

STRESS TESTING SYSTEM, LATERAL TILTING

K-Number: K790545 · 1979-06-06

ApplicantEngineering Dynamics Corp.
Decision Date1979-06-06
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STRESS TESTING SYSTEM, LATERAL TILTING 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 1979-06-06 under 510(k) number K790545. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRESS TESTING SYSTEM, LATERAL TILTING?

STRESS TESTING SYSTEM, LATERAL TILTING is a medical device that received FDA 510(k) clearance on 1979-06-06. The listed applicant is Engineering Dynamics Corp.. The 510(k) number is K790545.

When did STRESS TESTING SYSTEM, LATERAL TILTING receive FDA 510(k) clearance?

STRESS TESTING SYSTEM, LATERAL TILTING received FDA 510(k) clearance on 1979-06-06, under 510(k) number K790545.

Who is the listed applicant for STRESS TESTING SYSTEM, LATERAL TILTING?

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

What is the FDA product code for STRESS TESTING SYSTEM, LATERAL TILTING?

The FDA product code for STRESS TESTING SYSTEM, LATERAL TILTING is DRT.

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Other records listing Engineering Dynamics Corp. as applicant

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Related Devices (Code: DRT)

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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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