FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

NOVATECH TALCAIR

K Number: K170030 · Decision Mar 13, 2017
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
5
Review Days
68

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Basic Information

Device Name
NOVATECH TALCAIR
K Number
K170030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Novatech SA
Date Received
January 4, 2017
Decision Date
March 13, 2017
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

Similar 510(k) Clearances

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

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Other Clearances by Novatech SA

K Number Device Name
K242324 DUTAU-NOVATECH®
K243126 TRACHEOBRONXANE™ DUMON®
K151832 NOVATECH TALCAIR
K971509 ENDOXANE