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FDA 510(k)

LACRYTEST

K-Number: K034057 · 2004-03-09

ApplicantAdiatec SA
Decision Date2004-03-09
Product CodeDGC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LACRYTEST is the device name listed in this FDA 510(k) record. The listed applicant is Adiatec SA. It received FDA 510(k) clearance on 2004-03-09 under 510(k) number K034057. The device is classified under product code DGC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACRYTEST?

LACRYTEST is a medical device that received FDA 510(k) clearance on 2004-03-09. The listed applicant is Adiatec SA. The 510(k) number is K034057.

When did LACRYTEST receive FDA 510(k) clearance?

LACRYTEST received FDA 510(k) clearance on 2004-03-09, under 510(k) number K034057.

Who is the listed applicant for LACRYTEST?

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

What is the FDA product code for LACRYTEST?

The FDA product code for LACRYTEST is DGC.

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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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