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FDA 510(k)

LDS - LASER DELIVERY SYSTEM

K-Number: K862568 · 1986-10-07

ApplicantCoherent Medical Group
Decision Date1986-10-07
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LDS - LASER DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Coherent Medical Group. It received FDA 510(k) clearance on 1986-10-07 under 510(k) number K862568. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LDS - LASER DELIVERY SYSTEM?

LDS - LASER DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1986-10-07. The listed applicant is Coherent Medical Group. The 510(k) number is K862568.

When did LDS - LASER DELIVERY SYSTEM receive FDA 510(k) clearance?

LDS - LASER DELIVERY SYSTEM received FDA 510(k) clearance on 1986-10-07, under 510(k) number K862568.

Who is the listed applicant for LDS - LASER DELIVERY SYSTEM?

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

What is the FDA product code for LDS - LASER DELIVERY SYSTEM?

The FDA product code for LDS - LASER DELIVERY SYSTEM is HQF.

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Other records listing Coherent Medical Group 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.

K963339COHERENT ULTRAPULSE CO2 SURGICAL LASERSK960032COHERENT VERSAPULSE AESTHETIC SURGICAL LASERSK932981COHERENT VERSAPULSE 2.1 HOLMIUM SURGICAL LASERSK923575COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERSK932468NOVUS MULTIWAVELENGTHK930981ACCULITE(TM) OTOPROBE

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Related Devices (Code: HQF)

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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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