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

MULTIFOCUS COMPACT BTE HEARING AID

K Number: K933307 · Decision Aug 23, 1993
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
9
Review Days
47

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Basic Information

Device Name
MULTIFOCUS COMPACT BTE HEARING AID
K Number
K933307
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oticon, Inc.
Date Received
July 7, 1993
Decision Date
August 23, 1993
Product Code
ESD
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
ESD Hearing Aid, Air-Conduction, Prescription

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Other Clearances by Oticon, Inc.

K Number Device Name
K973885 OTICON DIGISOUND ITE
K973886 OTICON DIGISOUND COMPACT
K964683 DIGIFOCUS ITE
K961059 DIGIFOCUS COMPACT
K960284 OTICON /PRIMOFOCUS (PF)
K954794 OTICON
K950381 OTICON/LOGIC
K946045 OTICON