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FDA 510(k)

OCULIGHT SL/SLX

K-Number: K020374 · 2002-05-03

ApplicantIridex Corp
Decision Date2002-05-03
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCULIGHT SL/SLX is the device name listed in this FDA 510(k) record. The listed applicant is Iridex Corp. It received FDA 510(k) clearance on 2002-05-03 under 510(k) number K020374. 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 OCULIGHT SL/SLX?

OCULIGHT SL/SLX is a medical device that received FDA 510(k) clearance on 2002-05-03. The listed applicant is Iridex Corp. The 510(k) number is K020374.

When did OCULIGHT SL/SLX receive FDA 510(k) clearance?

OCULIGHT SL/SLX received FDA 510(k) clearance on 2002-05-03, under 510(k) number K020374.

Who is the listed applicant for OCULIGHT SL/SLX?

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

What is the FDA product code for OCULIGHT SL/SLX?

The FDA product code for OCULIGHT SL/SLX is HQF.

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Other records listing Iridex Corp 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.

K121475TXCELL SCANNING LASER DELIVERY SYSTEMK071687FAMILI OF IRIDEX IQ LASER SYSTEMSK062074IRIDEX WIRELESS FOOTSWITCHK062369IRIDEX OCULIGHT TXK060905IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1K050562OCULIGHT GL/GLX

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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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