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FDA 510(k)

TEMPLATE

K-Number: K873470 · 1987-09-08

ApplicantCox-Uphuff Intl.
Decision Date1987-09-08
Product CodeFTY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TEMPLATE 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 1987-09-08 under 510(k) number K873470. The device is classified under product code FTY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPLATE?

TEMPLATE is a medical device that received FDA 510(k) clearance on 1987-09-08. The listed applicant is Cox-Uphuff Intl.. The 510(k) number is K873470.

When did TEMPLATE receive FDA 510(k) clearance?

TEMPLATE received FDA 510(k) clearance on 1987-09-08, under 510(k) number K873470.

Who is the listed applicant for TEMPLATE?

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

What is the FDA product code for TEMPLATE?

The FDA product code for TEMPLATE is FTY.

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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, HYDROXYLAPATITEK865056CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDERK871200CUI NASAL SEPTUM BUTTONK865033BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDERK854339CUI CHIN SIZER

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Related Devices (Code: FTY)

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.

K160501Noxilizer Surgical RulerNoxilizer, Inc.K951064DISPOSABLE WOUND MEASURE GUIDE, PLASTIC, PROTECTOR, WOUND, PLASTICS-E Sales & Distribution, Inc.K934930OLYMPIC AUTO-LENGTHOlympic Medical Corp.K932112OLYMPIC INFA-LENGTHOlympic Medical Corp.K883485STRYKER PRESSURE MONITOR SYSTEMStryker Corp.K880441PEDIATRIC AIRWAY MEASUREMENT SYSTEM & P.A.M.S.Plane Iii, Inc.

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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