Cleared Traditional

K881963 - MSI 3002 SERIES BED
(FDA 510(k) Clearance)

K881963 · Med Service, Inc. · General Hospital

Jun 1988

Decision

49d

Days

Class 2

Risk

K881963 is an FDA 510(k) clearance for the MSI 3002 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 June 28, 1988, 49 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	K881963 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 10, 1988
Decision Date	June 28, 1988
Days to Decision	49 days
Submission Type	Traditional
Review Panel	General Hospital (HO)
Summary	—