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

MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES

K Number: K030857 · Decision Oct 16, 2003
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
3
Review Days
212

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Basic Information

Device Name
MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES
K Number
K030857
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
Mahe Intl., Inc.
Date Received
March 18, 2003
Decision Date
October 16, 2003
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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Other Clearances by Mahe Intl., Inc.

K Number Device Name
K991426 MAHE INSTRUMENTS
K942823 MAHE INSTRUMENTS