ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG
K-Number: K896314 · 1990-05-10
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Device Summary
Frequently Asked Questions
What is the ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG?
ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG is a medical device that received FDA 510(k) clearance on 1990-05-10. The listed applicant is Hgm Medical Laser Systems, Inc.. The 510(k) number is K896314.
When did ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG receive FDA 510(k) clearance?
ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG received FDA 510(k) clearance on 1990-05-10, under 510(k) number K896314.
Who is the listed applicant for ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG?
The FDA 510(k) record lists Hgm Medical Laser Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG?
The FDA product code for ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG 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 Hgm Medical Laser Systems, 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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