INTERCURE LTD. RESPI-LOW


codes

Device Classification Name

device, biofeedback

510(k) Number K000405
Device Name INTERCURE LTD. RESPI-LOW
Original Applicant
INTERCURE LTD.
555 13th st. n.w.
washington, 
DC 
20004 -1109

Original Contact jonathan s kahan
Regulation Number 882.5050
Classification Product Code
HCC  
Date Received 02/07/2000
Decision Date 05/17/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

Type Traditional
Reviewed by Third Party No

Combination Product

No