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FDA 510(k)

BARRAQUER-KRUMEICH REFRACTIVE SET

K-Number: K954058 · 1995-11-06

ApplicantEyetech M.V.A.
Decision Date1995-11-06
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BARRAQUER-KRUMEICH REFRACTIVE SET is the device name listed in this FDA 510(k) record. The listed applicant is Eyetech M.V.A.. It received FDA 510(k) clearance on 1995-11-06 under 510(k) number K954058. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRAQUER-KRUMEICH REFRACTIVE SET?

BARRAQUER-KRUMEICH REFRACTIVE SET is a medical device that received FDA 510(k) clearance on 1995-11-06. The listed applicant is Eyetech M.V.A.. The 510(k) number is K954058.

When did BARRAQUER-KRUMEICH REFRACTIVE SET receive FDA 510(k) clearance?

BARRAQUER-KRUMEICH REFRACTIVE SET received FDA 510(k) clearance on 1995-11-06, under 510(k) number K954058.

Who is the listed applicant for BARRAQUER-KRUMEICH REFRACTIVE SET?

The FDA 510(k) record lists Eyetech M.V.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARRAQUER-KRUMEICH REFRACTIVE SET?

The FDA product code for BARRAQUER-KRUMEICH REFRACTIVE SET is HNO.

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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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