FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

NASOPORE EAR

K Number: K070715 · Decision May 7, 2007
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
14
Applicant Total
9
Review Days
54

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Basic Information

Device Name
NASOPORE EAR
K Number
K070715
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polyganics B.V.,
Date Received
March 14, 2007
Decision Date
May 7, 2007
Product Code
NHB
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
NHB Polymer, Ear, Nose And Throat, Synthetic, Absorbable

Similar 510(k) Clearances

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

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Other Clearances by Polyganics B.V.,

K Number Device Name
K141816 HEMOPORE
K141423 NASOPORE-FD
K112267 NEUROLAC(R) NERVE GUIDE
K062540 NASOPORE EAR, MODELS ND04, ND05
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