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FDA 510(k)

LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT)

K-Number: K864975 · 1987-02-25

ApplicantLaserscope
Decision Date1987-02-25
Product CodeEWG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT) is the device name listed in this FDA 510(k) record. The listed applicant is Laserscope. It received FDA 510(k) clearance on 1987-02-25 under 510(k) number K864975. The device is classified under product code EWG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT)?

LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT) is a medical device that received FDA 510(k) clearance on 1987-02-25. The listed applicant is Laserscope. The 510(k) number is K864975.

When did LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT) receive FDA 510(k) clearance?

LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT) received FDA 510(k) clearance on 1987-02-25, under 510(k) number K864975.

Who is the listed applicant for LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT)?

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

What is the FDA product code for LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT)?

The FDA product code for LASERSCOPE OMNIPLUS PHOTOSURGICAL SYSTEM FOR (ENT) is EWG.

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 Laserscope 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.

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Related Devices (Code: EWG)

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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