ELECTRONIC EXERCISE #313-PULSE RATE
K-Number: K830282 · 1983-04-14
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Device Summary
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
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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