RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM
K-Number: K933140 · 1994-03-02
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Device Summary
Frequently Asked Questions
What is the RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM?
RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-02. The listed applicant is Laser Photonics, Inc.. The 510(k) number is K933140.
When did RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM receive FDA 510(k) clearance?
RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM received FDA 510(k) clearance on 1994-03-02, under 510(k) number K933140.
Who is the listed applicant for RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM?
The FDA 510(k) record lists Laser Photonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM?
The FDA product code for RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM 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 Laser Photonics, 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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