510(k) K881962

MSI 2005 SERIES BED by Med Service, Inc. — Product Code FNJ

K881962 is an FDA 510(k) premarket notification submitted by Med Service, Inc. for the device "MSI 2005 SERIES BED". The FDA issued a decision of Substantially Equivalent on June 3, 1988. The device falls under product code FNJ (Bed, Manual), a Class I device regulated under 21 CFR 880.5120. Med Service, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 1988
Date Received
May 10, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bed, Manual
Device Class
Class I
Regulation Number
880.5120
Review Panel
HO
Submission Type