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FDA 510(k)

KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY

K-Number: K896183 · 1990-02-02

ApplicantLaserscope
Decision Date1990-02-02
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Laserscope. It received FDA 510(k) clearance on 1990-02-02 under 510(k) number K896183. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY?

KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY is a medical device that received FDA 510(k) clearance on 1990-02-02. The listed applicant is Laserscope. The 510(k) number is K896183.

When did KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY receive FDA 510(k) clearance?

KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY received FDA 510(k) clearance on 1990-02-02, under 510(k) number K896183.

Who is the listed applicant for KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY?

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 KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY?

The FDA product code for KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY is GEX. This falls under the Gastroenterology category.

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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: GEX)

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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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