Cleared Traditional

HOSPITAL BED

K863748 · Global Medical Prods, Inc. · General Hospital
Oct 1986
Decision
15d
Days
Class 1
Risk

About This 510(k) Submission

K863748 is an FDA 510(k) clearance for the HOSPITAL BED, a Bed, Manual (Class I — General Controls, product code FNJ), submitted by Global Medical Prods, Inc. (Chicago, US). The FDA issued a Cleared decision on October 9, 1986, 15 days after receiving the submission on September 24, 1986. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5120.

Submission Details

510(k) Number K863748 FDA.gov
FDA Decision Cleared SESE
Date Received September 24, 1986
Decision Date October 09, 1986
Days to Decision 15 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary —

Device Classification

Product Code FNJ — Bed, Manual
Device Class Class I — General Controls
CFR Regulation 21 CFR 880.5120

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