FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

COLOSHIELD KIT

K Number: K855121 · Decision Jan 8, 1986
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
37
Review Days
16

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Basic Information

Device Name
COLOSHIELD KIT
K Number
K855121
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Deknatel, Inc.
Date Received
December 23, 1985
Decision Date
January 8, 1986
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

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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. →