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FDA 510(k)

CUI CHIN SIZER

K-Number: K854339 · 1985-11-15

ApplicantCox-Uphuff Intl.
Decision Date1985-11-15
Product Code
DecisionSubstantially Equivalent

Device Summary

CUI CHIN SIZER is the device name listed in this FDA 510(k) record. The listed applicant is Cox-Uphuff Intl.. It received FDA 510(k) clearance on 1985-11-15 under 510(k) number K854339. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUI CHIN SIZER?

CUI CHIN SIZER is a medical device that received FDA 510(k) clearance on 1985-11-15. The listed applicant is Cox-Uphuff Intl.. The 510(k) number is K854339.

When did CUI CHIN SIZER receive FDA 510(k) clearance?

CUI CHIN SIZER received FDA 510(k) clearance on 1985-11-15, under 510(k) number K854339.

Who is the listed applicant for CUI CHIN SIZER?

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

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.

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Other records listing Cox-Uphuff Intl. 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.

K874276CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDERK874342LIGATURE CARRIER/PACKER, HYDROXYLAPATITEK873470TEMPLATEK865056CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDERK871200CUI NASAL SEPTUM BUTTONK865033BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER

View all 11 devices →

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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