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

WELCH ALLYN BI-OTOSCOPE

K Number: K955043 · Decision Nov 14, 1995
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
55
Applicant Total
104
Review Days
11

Basic Information

Device Name
WELCH ALLYN BI-OTOSCOPE
K Number
K955043
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4770
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WELCH ALLYN, INC.
Date Received
November 3, 1995
Decision Date
November 14, 1995
Product Code
ERA
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
ERA Otoscope

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