510(k) K920704

STRYKER I.V. CADDY ACCESSORY DEVICE by Stryker Medical — Product Code FPO

K920704 is an FDA 510(k) premarket notification submitted by Stryker Medical for the device "STRYKER I.V. CADDY ACCESSORY DEVICE". The FDA issued a decision of Substantially Equivalent on March 23, 1992. The device falls under product code FPO (Stretcher, Wheeled), a Class II device regulated under 21 CFR 880.6910. Stryker Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 1992
Date Received
February 18, 1992
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