FDA 510(k) FDA class 1 Substantially Equivalent 🇳🇱 Netherlands

NASOPORE EAR, MODELS ND04, ND05

K Number: K062540 · Decision Oct 18, 2006
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
3
Applicant Total
9
Review Days
49

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NASOPORE EAR, MODELS ND04, ND05
K Number
K062540
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5220
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polyganics B.V.,
Date Received
August 30, 2006
Decision Date
October 18, 2006
Product Code
KCN
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KCN Ear Wick

Similar 510(k) Clearances

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

View all

Other Clearances by Polyganics B.V.,

K Number Device Name
K141816 HEMOPORE
K141423 NASOPORE-FD
K112267 NEUROLAC(R) NERVE GUIDE
K070715 NASOPORE EAR
K052099 NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZ
K050573 NEUROLAC NERVE GUIDE
K042811 VIVOSORB SHEET, MODEL FS01
K032115 NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03