XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15
K-Number: K861688 · 1986-10-03
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Device Summary
Frequently Asked Questions
What is the XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15?
XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15 is a medical device that received FDA 510(k) clearance on 1986-10-03. The listed applicant is Xanar, Inc.. The 510(k) number is K861688.
When did XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15 receive FDA 510(k) clearance?
XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15 received FDA 510(k) clearance on 1986-10-03, under 510(k) number K861688.
Who is the listed applicant for XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15?
The FDA 510(k) record lists Xanar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15?
The FDA product code for XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15 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 Xanar, 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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