LIGHTSCALPEL
K-Number: K123037 · 2012-11-29
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Device Summary
Frequently Asked Questions
What is the LIGHTSCALPEL?
LIGHTSCALPEL is a medical device that received FDA 510(k) clearance on 2012-11-29. The listed applicant is Lightscalpel, LLC. The 510(k) number is K123037.
When did LIGHTSCALPEL receive FDA 510(k) clearance?
LIGHTSCALPEL received FDA 510(k) clearance on 2012-11-29, under 510(k) number K123037.
Who is the listed applicant for LIGHTSCALPEL?
The FDA 510(k) record lists Lightscalpel, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGHTSCALPEL?
The FDA product code for LIGHTSCALPEL 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 Lightscalpel, LLC 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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