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

DEKNATEL(R) MICROFLEX OPHTHAL POLY SUTURE,MODIFIED

K Number: K911905 · Decision Jul 2, 1991
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
83
Applicant Total
37
Review Days
74

Basic Information

Device Name
DEKNATEL(R) MICROFLEX OPHTHAL POLY SUTURE,MODIFIED
K Number
K911905
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DEKNATEL, INC.
Date Received
April 19, 1991
Decision Date
July 2, 1991
Product Code
GAW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

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K Number Device Name
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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
K930739 SUTURES POLYPROP., POLYETHELINE, NYLON & SILK
K930738 SURGICAL SUTURES, PGL, GUT, DEKLENE, OPTHAMEND ETC
K926338 PLEUR-EVAC CARDIOTOMY RESERVOIR # CR-9400 & 9400F
K930740 SURGICAL SUTURE, NONABSORABLE STAINLESS STEEL
Search all 37 clearances from DEKNATEL, INC. →