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FDA 510(k)

IRIDEX WIRELESS FOOTSWITCH

K-Number: K062074 · 2006-11-14

ApplicantIridex Corp
Decision Date2006-11-14
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IRIDEX WIRELESS FOOTSWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Iridex Corp. It received FDA 510(k) clearance on 2006-11-14 under 510(k) number K062074. 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 IRIDEX WIRELESS FOOTSWITCH?

IRIDEX WIRELESS FOOTSWITCH is a medical device that received FDA 510(k) clearance on 2006-11-14. The listed applicant is Iridex Corp. The 510(k) number is K062074.

When did IRIDEX WIRELESS FOOTSWITCH receive FDA 510(k) clearance?

IRIDEX WIRELESS FOOTSWITCH received FDA 510(k) clearance on 2006-11-14, under 510(k) number K062074.

Who is the listed applicant for IRIDEX WIRELESS FOOTSWITCH?

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 IRIDEX WIRELESS FOOTSWITCH?

The FDA product code for IRIDEX WIRELESS FOOTSWITCH 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.

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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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