CERVICAL PILLOW— 510(k) K830350

Substantially Equivalent

Deip Enterprises, Inc.

FDA 510(k) clearance K830350 for CERVICAL PILLOW, Substantially Equivalent on 1983-03-09. Applicant: Deip Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: Deip Enterprises, Inc.
Product code: Code IQK
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1983-02-03
Decision date: 1983-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IQK

K930730 — DORMIE NECK SUPPORT SYSTEM1993-07-22
K926291 — SCHUL-TEC IMMOBILIZER1993-03-30
K895477 — NOVA PILLOW1990-01-10
K896042 — MEDICAL DISPOSABLE BEDDING1990-01-10
K882264 — BATTLE CREEK PILLOW1988-08-09

More clearances from Deip Enterprises, Inc.

K830348 — VINYL EXTRICATION COLLAR1983-03-09
K830349 — SAC-RO-FORM INSERT & BINDER1983-03-09
K830351 — DISPOSABLE EXTRICATION COLLAR1983-03-09

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