AQUAPLAST TIE DOWN DRESSING— 510(k) K943871

Name: FDA 510(k) clearance K943871
Creator: U.S. Food and Drug Administration
Published: 1994-09-30

Substantially Equivalent

Wfr/Aquaplast Corp.

FDA 510(k) clearance K943871 for AQUAPLAST TIE DOWN DRESSING, Substantially Equivalent on 1994-09-30. Applicant: Wfr/Aquaplast Corp.. Device class: 1.

Clearance details

Applicant: Wfr/Aquaplast Corp.
Product code: Code LZM
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1994-08-08
Decision date: 1994-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wyckoff, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LZM

view all

K885136 — GRAFT GUARD1989-02-06

More clearances from Wfr/Aquaplast Corp.

view all

K120916 — QFIX RADIOTHERAPY CHAIR2012-06-20
K060671 — KVUE IGRT TREATMENT TABLE TOP, RT-4551KV, KVUE INSERTS AND ACCESSORIES, VARIOUS2006-05-04
K032156 — ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT2003-09-02
K021124 — ACCUFIX TILTING RADIOTRANSLUCENT HEADHOLDER2002-07-02
K973370 — AQUAPLAST PALATAL STENT1997-12-02

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