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FDA 510(k)

SOLX 790 TITANIUM SAPPHIRE LASER

K-Number: K081774 · 2008-09-12

ApplicantSolx, Inc.
Decision Date2008-09-12
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLX 790 TITANIUM SAPPHIRE LASER is the device name listed in this FDA 510(k) record. The listed applicant is Solx, Inc.. It received FDA 510(k) clearance on 2008-09-12 under 510(k) number K081774. 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 SOLX 790 TITANIUM SAPPHIRE LASER?

SOLX 790 TITANIUM SAPPHIRE LASER is a medical device that received FDA 510(k) clearance on 2008-09-12. The listed applicant is Solx, Inc.. The 510(k) number is K081774.

When did SOLX 790 TITANIUM SAPPHIRE LASER receive FDA 510(k) clearance?

SOLX 790 TITANIUM SAPPHIRE LASER received FDA 510(k) clearance on 2008-09-12, under 510(k) number K081774.

Who is the listed applicant for SOLX 790 TITANIUM SAPPHIRE LASER?

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

What is the FDA product code for SOLX 790 TITANIUM SAPPHIRE LASER?

The FDA product code for SOLX 790 TITANIUM SAPPHIRE LASER is HQF.

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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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