Cleared Traditional

K881960 - MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74
(FDA 510(k) Clearance)

K881960 · Med Service, Inc. · General Hospital

Nov 1988

Decision

175d

Days

Class 2

Risk

K881960 is an FDA 510(k) clearance for the MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74. 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 November 1, 1988, 175 days after receiving the submission on May 10, 1988.

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

Submission Details

510(k) Number	K881960 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 10, 1988
Decision Date	November 01, 1988
Days to Decision	175 days
Submission Type	Traditional
Review Panel	General Hospital (HO)
Summary	—