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FDA 510(k)

ND:YAG LASER SPECTACLES, MST MODEL #YLS-5

K-Number: K883839 · 1988-12-09

Decision Date1988-12-09
Product CodeKYP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ND:YAG LASER SPECTACLES, MST MODEL #YLS-5 is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1988-12-09 under 510(k) number K883839. The device is classified under product code KYP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 28 devices →

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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