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FDA 510(k)

Q-SCAN THERMOGRAPHY SYSTEM

K-Number: K843124 · 1984-11-29

ApplicantQmax Medical, Inc.
Decision Date1984-11-29
Product CodeKXZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Q-SCAN THERMOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Qmax Medical, Inc.. It received FDA 510(k) clearance on 1984-11-29 under 510(k) number K843124. The device is classified under product code KXZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q-SCAN THERMOGRAPHY SYSTEM?

Q-SCAN THERMOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Qmax Medical, Inc.. The 510(k) number is K843124.

When did Q-SCAN THERMOGRAPHY SYSTEM receive FDA 510(k) clearance?

Q-SCAN THERMOGRAPHY SYSTEM received FDA 510(k) clearance on 1984-11-29, under 510(k) number K843124.

Who is the listed applicant for Q-SCAN THERMOGRAPHY SYSTEM?

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

What is the FDA product code for Q-SCAN THERMOGRAPHY SYSTEM?

The FDA product code for Q-SCAN THERMOGRAPHY SYSTEM is KXZ.

Related Clinical Trials

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Related Devices (Code: KXZ)

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.

K851034NOVATHERMMedtech Products, Inc.K832731BREAST & BODY HEALTH SYSTEM 2000American Thermal Instruments, Inc.K813547THERMASCANBcd Products, Inc.K781916FLEXT-THERME-Z-Em, Inc.K770986FLEXI-THERM FILME-Z-Em, Inc.K770678ELC-THERMO-SYSTEMCutter Laboratories, Inc.

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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