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FDA 510(k)

QUANTUM

K-Number: K896408 · 1990-09-20

ApplicantStressmaster Systems, Inc.
Decision Date1990-09-20
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

QUANTUM is the device name listed in this FDA 510(k) record. The listed applicant is Stressmaster Systems, Inc.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K896408. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTUM?

QUANTUM is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Stressmaster Systems, Inc.. The 510(k) number is K896408.

When did QUANTUM receive FDA 510(k) clearance?

QUANTUM received FDA 510(k) clearance on 1990-09-20, under 510(k) number K896408.

Who is the listed applicant for QUANTUM?

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

What is the FDA product code for QUANTUM?

The FDA product code for QUANTUM is GZJ.

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Related Devices (Code: GZJ)

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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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