Cleared Traditional

K881782 - MSI 4000 SERIES BED
(FDA 510(k) Clearance)

K881782 · Med Service, Inc. · General Hospital

Jul 1988

Decision

77d

Days

Class 2

Risk

K881782 is an FDA 510(k) clearance for the MSI 4000 SERIES BED. This device is classified as a Bed, Ac-powered Adjustable Hospital (Class II — Special Controls, product code FNL).

Submitted by Med Service, Inc. (Batesville, US). The FDA issued a Cleared decision on July 12, 1988, 77 days after receiving the submission on April 26, 1988.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5100.

Submission Details

510(k) Number	K881782 FDA.gov
FDA Decision	Cleared SESE
Date Received	April 26, 1988
Decision Date	July 12, 1988
Days to Decision	77 days
Submission Type	Traditional
Review Panel	General Hospital (HO)
Summary	—