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FDA 510(k)

MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY

K-Number: K953174 · 1995-08-28

Decision Date1995-08-28
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Microquartz Medical, Inc.. It received FDA 510(k) clearance on 1995-08-28 under 510(k) number K953174. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY?

MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY is a medical device that received FDA 510(k) clearance on 1995-08-28. The listed applicant is Microquartz Medical, Inc.. The 510(k) number is K953174.

When did MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY receive FDA 510(k) clearance?

MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY received FDA 510(k) clearance on 1995-08-28, under 510(k) number K953174.

Who is the listed applicant for MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY?

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

What is the FDA product code for MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY?

The FDA product code for MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY is GEX. This falls under the Gastroenterology category.

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 Microquartz Medical, Inc. 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: GEX)

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

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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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