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FDA 510(k)

ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY

K-Number: K875042 · 1988-06-24

Decision Date1988-06-24
Product CodeLKW
DecisionSubstantially Equivalent

Device Summary

ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY is the device name listed in this FDA 510(k) record. The listed applicant is Surgilase, Inc.. It received FDA 510(k) clearance on 1988-06-24 under 510(k) number K875042. The device is classified under product code LKW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY?

ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY is a medical device that received FDA 510(k) clearance on 1988-06-24. The listed applicant is Surgilase, Inc.. The 510(k) number is K875042.

When did ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY receive FDA 510(k) clearance?

ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY received FDA 510(k) clearance on 1988-06-24, under 510(k) number K875042.

Who is the listed applicant for ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY?

The FDA 510(k) record lists Surgilase, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY?

The FDA product code for ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY 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.

Other records listing Surgilase, 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.

View all 19 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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