MODEL 5000 MULTIPLACE HYPERBARIC THERAPY


information about

Device Classification Name

chamber, hyperbaric

510(k) Number K002794
Device Name MODEL 5000 MULTIPLACE HYPERBARIC THERAPY
Original Applicant
HYPERTEC, INC.
po box 7007
deerfield, 
IL 
60015

Original Contact daniel kamm
Regulation Number 868.5470
Classification Product Code
CBF  
Date Received 09/07/2000
Decision Date 12/06/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

Anesthesiology

Type Traditional
Reviewed by Third Party No

Combination Product

No