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FDA 510(k)

LIGHT COAGULATOR LC 250

K-Number: K881334 · 1989-11-16

ApplicantNk-Optik GmbH
Decision Date1989-11-16
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHT COAGULATOR LC 250 is the device name listed in this FDA 510(k) record. The listed applicant is Nk-Optik GmbH. It received FDA 510(k) clearance on 1989-11-16 under 510(k) number K881334. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT COAGULATOR LC 250?

LIGHT COAGULATOR LC 250 is a medical device that received FDA 510(k) clearance on 1989-11-16. The listed applicant is Nk-Optik GmbH. The 510(k) number is K881334.

When did LIGHT COAGULATOR LC 250 receive FDA 510(k) clearance?

LIGHT COAGULATOR LC 250 received FDA 510(k) clearance on 1989-11-16, under 510(k) number K881334.

Who is the listed applicant for LIGHT COAGULATOR LC 250?

The FDA 510(k) record lists Nk-Optik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHT COAGULATOR LC 250?

The FDA product code for LIGHT COAGULATOR LC 250 is HAM.

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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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