510(k) K942948

STRYKER POWERED STRETCHER by Stryker Corp. — Product Code FPO

K942948 is an FDA 510(k) premarket notification submitted by Stryker Corp. for the device "STRYKER POWERED STRETCHER". The FDA issued a decision of Substantially Equivalent on January 24, 1995. The device falls under product code FPO (Stretcher, Wheeled), a Class II device regulated under 21 CFR 880.6910. Stryker Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1995
Date Received
June 23, 1994
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