FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

NASOSTAT

K Number: K781615 · Decision Oct 11, 1978
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
46
Applicant Total
1
Review Days
20

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Basic Information

Device Name
NASOSTAT
K Number
K781615
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4100
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Nasostat, Inc.
Date Received
September 21, 1978
Decision Date
October 11, 1978
Product Code
EMX
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
EMX Balloon, Epistaxis

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