Cleared Traditional

K881962 - MSI 2005 SERIES BED
(FDA 510(k) Clearance)

K881962 · Med Service, Inc. · General Hospital

Jun 1988

Decision

24d

Days

Class 1

Risk

K881962 is an FDA 510(k) clearance for the MSI 2005 SERIES BED. This device is classified as a Bed, Manual (Class I — General Controls, product code FNJ).

Submitted by Med Service, Inc. (Batesville, US). The FDA issued a Cleared decision on June 3, 1988, 24 days after receiving the submission on May 10, 1988.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5120.

Submission Details

510(k) Number	K881962 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 10, 1988
Decision Date	June 03, 1988
Days to Decision	24 days
Submission Type	Traditional
Review Panel	General Hospital (HO)
Summary	—