FDA 510(k)

ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR

K-Number: K853460 · 1985-09-05

Decision Date1985-09-05

Product Code

DecisionSubstantially Equivalent

Device Summary

ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Heraeus, Inc.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K853460. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR?

ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Heraeus, Inc.. The 510(k) number is K853460.

When did ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR receive FDA 510(k) clearance?

ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR received FDA 510(k) clearance on 1985-09-05, under 510(k) number K853460.

Who is the listed applicant for ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR?

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

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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.