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FDA 510(k)

ELECTRONIC EXERCISE #313-PULSE RATE

K-Number: K830282 · 1983-04-14

Decision Date1983-04-14
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC EXERCISE #313-PULSE RATE is the device name listed in this FDA 510(k) record. The listed applicant is Walton Manufacturer Co.. It received FDA 510(k) clearance on 1983-04-14 under 510(k) number K830282. 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 ELECTRONIC EXERCISE #313-PULSE RATE?

ELECTRONIC EXERCISE #313-PULSE RATE is a medical device that received FDA 510(k) clearance on 1983-04-14. The listed applicant is Walton Manufacturer Co.. The 510(k) number is K830282.

When did ELECTRONIC EXERCISE #313-PULSE RATE receive FDA 510(k) clearance?

ELECTRONIC EXERCISE #313-PULSE RATE received FDA 510(k) clearance on 1983-04-14, under 510(k) number K830282.

Who is the listed applicant for ELECTRONIC EXERCISE #313-PULSE RATE?

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

What is the FDA product code for ELECTRONIC EXERCISE #313-PULSE RATE?

The FDA product code for ELECTRONIC EXERCISE #313-PULSE RATE is DRT.

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.

Related Devices (Code: DRT)

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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