STRESS SYSTEM, SINGLE-CHANNEL (#21125)
K-Number: K760463 · 1976-08-30
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Device Summary
Frequently Asked Questions
What is the STRESS SYSTEM, SINGLE-CHANNEL (#21125)?
STRESS SYSTEM, SINGLE-CHANNEL (#21125) is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K760463.
When did STRESS SYSTEM, SINGLE-CHANNEL (#21125) receive FDA 510(k) clearance?
STRESS SYSTEM, SINGLE-CHANNEL (#21125) received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760463.
Who is the listed applicant for STRESS SYSTEM, SINGLE-CHANNEL (#21125)?
The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRESS SYSTEM, SINGLE-CHANNEL (#21125)?
The FDA product code for STRESS SYSTEM, SINGLE-CHANNEL (#21125) is DPS.
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 Hewlett-Packard Co. 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.
Related Devices (Code: DPS)
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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