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FDA 510(k)

ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080&

K-Number: K823402 · 1982-12-26

Decision Date1982-12-26
Product CodeCDQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080& is the device name listed in this FDA 510(k) record. The listed applicant is Emd Chemicals, Inc.. It received FDA 510(k) clearance on 1982-12-26 under 510(k) number K823402. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080&?

ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080& is a medical device that received FDA 510(k) clearance on 1982-12-26. The listed applicant is Emd Chemicals, Inc.. The 510(k) number is K823402.

When did ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080& receive FDA 510(k) clearance?

ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080& received FDA 510(k) clearance on 1982-12-26, under 510(k) number K823402.

Who is the listed applicant for ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080&?

The FDA 510(k) record lists Emd Chemicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080&?

The FDA product code for ULTRACHEM BUN-UV-GEM SAEC APPLI.#65080& is CDQ.

Related Clinical Trials

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.

Other records listing Emd Chemicals, Inc. as applicant

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.

View all 62 devices →

Related Devices (Code: CDQ)

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.

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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