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FDA 510(k)

TREADMILL STRESS EXERCISE SYSTEM

K-Number: K770240 · 1977-02-14

ApplicantBurdick Corp.
Decision Date1977-02-14
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TREADMILL STRESS EXERCISE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1977-02-14 under 510(k) number K770240. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREADMILL STRESS EXERCISE SYSTEM?

TREADMILL STRESS EXERCISE SYSTEM is a medical device that received FDA 510(k) clearance on 1977-02-14. The listed applicant is Burdick Corp.. The 510(k) number is K770240.

When did TREADMILL STRESS EXERCISE SYSTEM receive FDA 510(k) clearance?

TREADMILL STRESS EXERCISE SYSTEM received FDA 510(k) clearance on 1977-02-14, under 510(k) number K770240.

Who is the listed applicant for TREADMILL STRESS EXERCISE SYSTEM?

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

What is the FDA product code for TREADMILL STRESS EXERCISE SYSTEM?

The FDA product code for TREADMILL STRESS EXERCISE SYSTEM is IOL.

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 Burdick 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.

View all 38 devices →

Related Devices (Code: IOL)

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

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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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