FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇷 Costa Rica

PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI

K Number: K896697 · Decision Feb 8, 1990
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
47
Applicant Total
37
Review Days
72

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Basic Information

Device Name
PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI
K Number
K896697
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Deknatel, Inc.
Date Received
November 28, 1989
Decision Date
February 8, 1990
Product Code
KDQ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDQ Bottle, Collection, Vacuum

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Other Clearances by Deknatel, Inc.

K Number Device Name
K963850 PLEUR-EVAC SAHARA PLUS MODEL S-1150 CONTINUOUS REINFUSION AUTOTRANSFUSION SYSTEM
K962683 SNOWDEN-PENCER COMPUTERIZED HIGH FLOW INSUFFLATOR
K964070 DEKNATEL DSP PLEUR-EVAC AUTOTRANSFUSION BLOOD RECOVERY BAG
K963098 PLEUR-EVAC SHARA PLUS MODEL S-2150/CONTINUOUS REINFUSION AUTOTRANSFUSION SYSTEM(S-100)
K962856 PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTR
K925243 DEKNATEL(TM) PLEUR-EVAC(R) THORACIC CATHETER
K930738 SURGICAL SUTURES, PGL, GUT, DEKLENE, OPTHAMEND ETC
K930740 SURGICAL SUTURE, NONABSORABLE STAINLESS STEEL
K930739 SUTURES POLYPROP., POLYETHELINE, NYLON & SILK
K926338 PLEUR-EVAC CARDIOTOMY RESERVOIR # CR-9400 & 9400F
Search all 37 clearances from Deknatel, Inc. →