ND:YAG LASER SPECTACLES, MST MODEL #YLS-5
K-Number: K883839 · 1988-12-09
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Device Summary
Frequently Asked Questions
What is the ND:YAG LASER SPECTACLES, MST MODEL #YLS-5?
ND:YAG LASER SPECTACLES, MST MODEL #YLS-5 is a medical device that received FDA 510(k) clearance on 1988-12-09. The listed applicant is Marlo Surgical Technology. The 510(k) number is K883839.
When did ND:YAG LASER SPECTACLES, MST MODEL #YLS-5 receive FDA 510(k) clearance?
ND:YAG LASER SPECTACLES, MST MODEL #YLS-5 received FDA 510(k) clearance on 1988-12-09, under 510(k) number K883839.
Who is the listed applicant for ND:YAG LASER SPECTACLES, MST MODEL #YLS-5?
The FDA 510(k) record lists Marlo Surgical Technology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ND:YAG LASER SPECTACLES, MST MODEL #YLS-5?
The FDA product code for ND:YAG LASER SPECTACLES, MST MODEL #YLS-5 is KYP.
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 Marlo Surgical Technology 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: KYP)
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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