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FDA 510(k)

STRESS TABLE/ERGOMETER SYSTEM

K-Number: K792591 · 1980-01-04

Decision Date1980-01-04
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STRESS TABLE/ERGOMETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1980-01-04 under 510(k) number K792591. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRESS TABLE/ERGOMETER SYSTEM?

STRESS TABLE/ERGOMETER SYSTEM is a medical device that received FDA 510(k) clearance on 1980-01-04. The listed applicant is Victoreen, Inc.. The 510(k) number is K792591.

When did STRESS TABLE/ERGOMETER SYSTEM receive FDA 510(k) clearance?

STRESS TABLE/ERGOMETER SYSTEM received FDA 510(k) clearance on 1980-01-04, under 510(k) number K792591.

Who is the listed applicant for STRESS TABLE/ERGOMETER SYSTEM?

The FDA 510(k) record lists Victoreen, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRESS TABLE/ERGOMETER SYSTEM?

The FDA product code for STRESS TABLE/ERGOMETER SYSTEM is ISD.

Related Clinical Trials

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.

Other records listing Victoreen, 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.

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Related Devices (Code: ISD)

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.

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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