FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

FTRD System Set

K Number: K170867 · Decision Jul 25, 2017
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
62
Applicant Total
14
Review Days
124

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Basic Information

Device Name
FTRD System Set
K Number
K170867
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4400
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ovesco Endoscopy AG
Date Received
March 23, 2017
Decision Date
July 25, 2017
Product Code
PKL
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
PKL Hemostatic Metal Clip For The Gi Tract

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PKL), ordered by most recent decision date.

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Other Clearances by Ovesco Endoscopy AG

K Number Device Name
K251562 OTSCneo System Set (100.03n-14n, 100.27n-31n)
K242586 ArgoCap (200.52)
K241858 BARS Set (100.60)
K221385 LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)
K200684 gastroduodenal FTRD Set
K183309 stentfix OTSC System Set
DEN160014 remOVE System
K153550 FTRD System Set
K150067 OTSC Proctology
K141790 AQANIFE
Search all 14 clearances from Ovesco Endoscopy AG →