FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NASAL/PARANASAL ENDOSCOPE

K Number: K930931 · Decision May 17, 1993
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
156
Applicant Total
101
Review Days
83

Basic Information

Device Name
NASAL/PARANASAL ENDOSCOPE
K Number
K930931
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4760
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STORZ INSTRUMENT CO.
Date Received
February 23, 1993
Decision Date
May 17, 1993
Product Code
EOB
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
EOB Nasopharyngoscope (Flexible Or Rigid)

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