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FDA 510(k)

CALSSIQUE OR MYSTIQUE

K-Number: K932978 · 1993-12-22

ApplicantDekumed, Kunststofftechnik Degler GmbH
Decision Date1993-12-22
Product CodeKCZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CALSSIQUE OR MYSTIQUE is the device name listed in this FDA 510(k) record. The listed applicant is Dekumed, Kunststofftechnik Degler GmbH. It received FDA 510(k) clearance on 1993-12-22 under 510(k) number K932978. The device is classified under product code KCZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALSSIQUE OR MYSTIQUE?

CALSSIQUE OR MYSTIQUE is a medical device that received FDA 510(k) clearance on 1993-12-22. The listed applicant is Dekumed, Kunststofftechnik Degler GmbH. The 510(k) number is K932978.

When did CALSSIQUE OR MYSTIQUE receive FDA 510(k) clearance?

CALSSIQUE OR MYSTIQUE received FDA 510(k) clearance on 1993-12-22, under 510(k) number K932978.

Who is the listed applicant for CALSSIQUE OR MYSTIQUE?

The FDA 510(k) record lists Dekumed, Kunststofftechnik Degler GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALSSIQUE OR MYSTIQUE?

The FDA product code for CALSSIQUE OR MYSTIQUE is KCZ.

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Related Devices (Code: KCZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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