Cleared Traditional

HARE EMERGENCY STRETCHER

K900670 · Dyna Corp. · General Hospital
Apr 1990
Decision
69d
Days
Class 1
Risk

About This 510(k) Submission

K900670 is an FDA 510(k) clearance for the HARE EMERGENCY STRETCHER, a Stretcher, Hand-carried (Class I — General Controls, product code FPP), submitted by Dyna Corp. (Carlsbad, US). The FDA issued a Cleared decision on April 23, 1990, 69 days after receiving the submission on February 13, 1990. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.6900.

Submission Details

510(k) Number K900670 FDA.gov
FDA Decision Cleared SESE
Date Received February 13, 1990
Decision Date April 23, 1990
Days to Decision 69 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary —

Device Classification

Product Code FPP — Stretcher, Hand-carried
Device Class Class I — General Controls
CFR Regulation 21 CFR 880.6900