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FDA 510(k)

ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2

K-Number: K121724 · 2012-09-20

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date2012-09-20
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2012-09-20 under 510(k) number K121724. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2?

ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 is a medical device that received FDA 510(k) clearance on 2012-09-20. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K121724.

When did ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 receive FDA 510(k) clearance?

ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 received FDA 510(k) clearance on 2012-09-20, under 510(k) number K121724.

Who is the listed applicant for ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2?

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

What is the FDA product code for ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2?

The FDA product code for ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 is FCW.

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Related Devices (Code: FCW)

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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