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FDA 510(k)

LIGHTWRITER

K-Number: K931855 · 1994-05-10

ApplicantZygo Corp.
Decision Date1994-05-10
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIGHTWRITER is the device name listed in this FDA 510(k) record. The listed applicant is Zygo Corp.. It received FDA 510(k) clearance on 1994-05-10 under 510(k) number K931855. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHTWRITER?

LIGHTWRITER is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Zygo Corp.. The 510(k) number is K931855.

When did LIGHTWRITER receive FDA 510(k) clearance?

LIGHTWRITER received FDA 510(k) clearance on 1994-05-10, under 510(k) number K931855.

Who is the listed applicant for LIGHTWRITER?

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

What is the FDA product code for LIGHTWRITER?

The FDA product code for LIGHTWRITER is ILQ.

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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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