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FDA 510(k)

COMPUSTRESS STRESS TESTING SYS

K-Number: K842339 · 1984-12-19

ApplicantIntl. Medical, Inc.
Decision Date1984-12-19
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COMPUSTRESS STRESS TESTING SYS is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical, Inc.. It received FDA 510(k) clearance on 1984-12-19 under 510(k) number K842339. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUSTRESS STRESS TESTING SYS?

COMPUSTRESS STRESS TESTING SYS is a medical device that received FDA 510(k) clearance on 1984-12-19. The listed applicant is Intl. Medical, Inc.. The 510(k) number is K842339.

When did COMPUSTRESS STRESS TESTING SYS receive FDA 510(k) clearance?

COMPUSTRESS STRESS TESTING SYS received FDA 510(k) clearance on 1984-12-19, under 510(k) number K842339.

Who is the listed applicant for COMPUSTRESS STRESS TESTING SYS?

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

What is the FDA product code for COMPUSTRESS STRESS TESTING SYS?

The FDA product code for COMPUSTRESS STRESS TESTING SYS is DQK.

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Other records listing Intl. Medical, Inc. as applicant

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Related Devices (Code: DQK)

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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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