COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS
K-Number: K923575 · 1993-09-29
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Device Summary
Frequently Asked Questions
What is the COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS?
COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is Coherent Medical Group. The 510(k) number is K923575.
When did COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS receive FDA 510(k) clearance?
COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS received FDA 510(k) clearance on 1993-09-29, under 510(k) number K923575.
Who is the listed applicant for COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS?
The FDA 510(k) record lists Coherent Medical Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS?
The FDA product code for COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS 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 Coherent Medical Group 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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