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FDA 510(k)

SIGMA-BRILLEN (OR) MULTIPLE

K-Number: K930956 · 1993-10-20

ApplicantSigma-Brillen
Decision Date1993-10-20
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SIGMA-BRILLEN (OR) MULTIPLE is the device name listed in this FDA 510(k) record. The listed applicant is Sigma-Brillen. It received FDA 510(k) clearance on 1993-10-20 under 510(k) number K930956. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGMA-BRILLEN (OR) MULTIPLE?

SIGMA-BRILLEN (OR) MULTIPLE is a medical device that received FDA 510(k) clearance on 1993-10-20. The listed applicant is Sigma-Brillen. The 510(k) number is K930956.

When did SIGMA-BRILLEN (OR) MULTIPLE receive FDA 510(k) clearance?

SIGMA-BRILLEN (OR) MULTIPLE received FDA 510(k) clearance on 1993-10-20, under 510(k) number K930956.

Who is the listed applicant for SIGMA-BRILLEN (OR) MULTIPLE?

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

What is the FDA product code for SIGMA-BRILLEN (OR) MULTIPLE?

The FDA product code for SIGMA-BRILLEN (OR) MULTIPLE is HQZ.

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Related Devices (Code: HQZ)

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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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