BABY POD


Device Classification Name

stretcher, hand-carried

510(k) Number K030283
Device Name BABY POD
Original Applicant
PRISM ENTERPRISES, INC.
p.o. box 560
stillwater, 
MN 
55082

Original Contact elaine duncan
Regulation Number 880.6900
Classification Product Code
FPP  
Date Received 01/27/2003
Decision Date 04/22/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No