Battle Creek Pillow

FDA 510(k) K882264 · Battle Creek Equipment Co.

Substantially Equivalent

510(k) numberK882264

Submission

Device name
Battle Creek Pillow
Applicant
Battle Creek Equipment Co.
Battle Creek, MI, US
Received
May 31, 1988
Decision date
August 9, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IQK – Orthosis, Cervical
Device class
Class I (low risk)
Regulation
21 CFR 890.3490
Specialty
Physical Medicine

Other 510(k)s with product code IQK

510(k)DeviceApplicantDecision
K930730Dormie Neck Support SystemIQK · Traditional The Western Diagnostics Co.07/22/1993SE
K926291Schul-Tec ImmobilizerIQK · Traditional Medical Emergency Support Equipment03/30/1993SE
K896042Medical Disposable BeddingIQK · Traditional Keystone Veterinary Supplies, Inc.01/10/1990SE
K895477Nova PillowIQK · Traditional Nova Health Systems, Inc.01/10/1990SE
K850465Cervical Collars & Head HaltersIQK · Traditional Abco Dealers, Inc.04/25/1985SE
K832990Stifnick Immobilizing CollarIQK · Traditional Laerdal California, Inc.11/07/1983SE
K832001Head-ImmobilizerIQK · Traditional Int'L Safety Corp.07/12/1983SE
K831582Vari-Support Neck Posture PillowIQK · Traditional Body Therapeutics, Inc.06/15/1983SE
K830351Disposable Extrication CollarIQK · Traditional Deip Enterprises, Inc.03/09/1983SE
K830350Cervical PillowIQK · Traditional Deip Enterprises, Inc.03/09/1983SE

More from Deip Enterprises, Inc.

510(k)DeviceDecision
K863884Pulsestar Exercise BikeISD · Traditional 10/23/1986SE
K854147Battle Creek Boardwalker Electric TreadmillIOL · Traditional 12/27/1985SE
K854148Battle Creek Digi-Tracker Elctric TreadmillIOL · Traditional 12/17/1985SE
K851237Thermophore Electric Fomentation UnitIRT · Traditional 07/29/1985SE
K840280Road Runner Electric TreadmillIOL · Traditional 02/04/1984SE
K791866Standard Health Bike Model 019ISD · Traditional 10/04/1979SE

Questions and answers

When was Battle Creek Pillow cleared by the FDA?

Battle Creek Pillow (K882264) received a 510(k) decision of Substantially Equivalent on August 9, 1988, 70 days after the submission was received.

What is the product code of K882264?

The FDA product code is IQK – Orthosis, Cervical, a Class I (low risk) device regulated under 21 CFR 890.3490.