FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DEKNA BAND KIT

K Number: K862115 · Decision Aug 19, 1986
Classifications
1
FEI Numbers
239
Registration Numbers
239
Same Product Code
36
Applicant Total
37
Review Days
77

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Basic Information

Device Name
DEKNA BAND KIT
K Number
K862115
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Deknatel, Inc.
Date Received
June 3, 1986
Decision Date
August 19, 1986
Product Code
ITG
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ITG Bandage, Cast

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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. →