510(k) K022309

STRYKER POWERED WHEELED STRETCHER by Stryker Corp. — Product Code INK

K022309 is an FDA 510(k) premarket notification submitted by Stryker Corp. for the device "STRYKER POWERED WHEELED STRETCHER". The FDA issued a decision of Substantially Equivalent on November 8, 2002. The device falls under product code INK (Stretcher, Wheeled, Powered), a Class II device regulated under 21 CFR 890.3690. Stryker Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 2002
Date Received
July 16, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stretcher, Wheeled, Powered
Device Class
Class II
Regulation Number
890.3690
Review Panel
PM
Submission Type