25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY
K-Number: K864166 · 1987-02-10
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Device Summary
Frequently Asked Questions
What is the 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY?
25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Weck Surgical Systems. The 510(k) number is K864166.
When did 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY receive FDA 510(k) clearance?
25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY received FDA 510(k) clearance on 1987-02-10, under 510(k) number K864166.
Who is the listed applicant for 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY?
The FDA 510(k) record lists Weck Surgical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY?
The FDA product code for 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY is LKW.
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.
Related Devices (Code: LKW)
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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