MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS


Device Classification Name

chamber, hyperbaric

510(k) Number K002795
Device Name MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS
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