TEMPLATE— 510(k) K873470

Substantially Equivalent

Cox-Uphuff Intl.

FDA 510(k) clearance K873470 for TEMPLATE, Substantially Equivalent on 1987-09-08. Applicant: Cox-Uphuff Intl.. Device class: 1.

Clearance details

Applicant: Cox-Uphuff Intl.
Product code: Code FTY
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-08-28
Decision date: 1987-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Cox-Uphuff Intl.

K874276 — CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER1987-12-02
K874342 — LIGATURE CARRIER/PACKER, HYDROXYLAPATITE1987-11-13
K865056 — CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER1987-05-22
K871200 — CUI NASAL SEPTUM BUTTON1987-04-15
K865033 — BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER1987-01-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.