TRIANGULAR BANDAGE CAT.#191— 510(k) K802006

Name: FDA 510(k) clearance K802006
Creator: U.S. Food and Drug Administration
Published: 1980-09-16

Substantially Equivalent

Pollak (Intl.), Ltd.

FDA 510(k) clearance K802006 for TRIANGULAR BANDAGE CAT.#191, Substantially Equivalent on 1980-09-16. Applicant: Pollak (Intl.), Ltd.. Device class: 1.

Clearance details

Applicant: Pollak (Intl.), Ltd.
Product code: Code ILI
Device class: Class 1
Regulation: 21 CFR 890.3640
Advisory panel: Physical Medicine
Date received: 1980-08-20
Decision date: 1980-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ILI

view all

K912661 — MATRX, PYRAMID TRIANGLE BANDAGE1991-08-21
K831549 — ARM SLINGS1983-06-30
K831706 — SATO FAMILY FIRST AID KIT1983-06-24
K823808 — VARIOUS ARM SLING1983-01-14
K823810 — A.C. SPLINT1983-01-14

More clearances from Pollak (Intl.), Ltd.

view all

K000227 — UMBICUT2000-04-27
K810049 — PEDICAT*1981-04-21
K810050 — VECAFIX*1981-03-26
K802009 — FLOWCLAMP CAT.#1011 & 10121980-10-31
K802011 — INFUSSION ALARM SYSTEM I.A.S. CAT.#11181980-10-31

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