Cleared Traditional

K831582 - VARI-SUPPORT NECK POSTURE PILLOW (FDA 510(k) Clearance)

Jun 1983
Decision
29d
Days
Class 1
Risk

K831582 is an FDA 510(k) clearance for the VARI-SUPPORT NECK POSTURE PILLOW. This device is classified as a Orthosis, Cervical (Class I - General Controls, product code IQK).

Submitted by Body Therapeutics, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 15, 1983, 29 days after receiving the submission on May 17, 1983.

This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3490.

Submission Details

510(k) Number K831582 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 17, 1983
Decision Date June 15, 1983
Days to Decision 29 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary

Device Classification

Product Code IQK — Orthosis, Cervical
Device Class Class I - General Controls
CFR Regulation 21 CFR 890.3490