MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER
K-Number: K950710 · 1995-03-10
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Device Summary
Frequently Asked Questions
What is the MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER?
MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER is a medical device that received FDA 510(k) clearance on 1995-03-10. The listed applicant is Microquartz Medical, Inc.. The 510(k) number is K950710.
When did MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER receive FDA 510(k) clearance?
MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER received FDA 510(k) clearance on 1995-03-10, under 510(k) number K950710.
Who is the listed applicant for MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER?
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 MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER?
The FDA product code for MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER 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
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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