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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name chamber, hyperbaric
510(k) Number K933929
Device Name LAB-SITE(R) SAFETY CANNULA
Applicant
MIGADA, LTD.
P.O. BOX 2
ASHDOD 77100
ISRAEL,  IL
Applicant Contact H. LEINWAND
Correspondent
MIGADA, LTD.
P.O. BOX 2
ASHDOD 77100
ISRAEL,  IL
Correspondent Contact H. LEINWAND
Regulation Number868.5470
Classification Product Code
CBF  
Date Received08/10/1993
Decision Date 12/07/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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