FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇷 Costa Rica

DEKNATEL HIGH PRECISION VASCULAR PUNCH(TM)

K Number: K890432 · Decision Apr 13, 1989
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
37
Review Days
76

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Basic Information

Device Name
DEKNATEL HIGH PRECISION VASCULAR PUNCH(TM)
K Number
K890432
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Deknatel, Inc.
Date Received
January 27, 1989
Decision Date
April 13, 1989
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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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. →