510(k) K854304

KEYMED OFFICE COUCH by Keymed, Inc. — Product Code FPO

K854304 is an FDA 510(k) premarket notification submitted by Keymed, Inc. for the device "KEYMED OFFICE COUCH". The FDA issued a decision of Substantially Equivalent on November 12, 1985. The device falls under product code FPO (Stretcher, Wheeled), a Class II device regulated under 21 CFR 880.6910. Keymed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 12, 1985
Date Received
October 25, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stretcher, Wheeled
Device Class
Class II
Regulation Number
880.6910
Review Panel
HO
Submission Type