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

PHILIPS P74P BEHIND-THE-EAR HEARING AID

K Number: K915252 · Decision Dec 5, 1991
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
20
Review Days
17

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Basic Information

Device Name
PHILIPS P74P BEHIND-THE-EAR HEARING AID
K Number
K915252
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Philips Hearing Instruments Co.
Date Received
November 18, 1991
Decision Date
December 5, 1991
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 Philips Hearing Instruments Co.

K Number Device Name
K972818 D72 DIGITAL
K971804 PHILIPS S1694, S1695
K965088 M11 SERIES: M11, M11M
K961770 PHILIPS 71 SERIES
K952658 HEARING AID
K944404 MO4 SERIES
K943670 MO6 SERIES
K943395 PHILIPS M38 SERIES
K942164 PHILIPS 61 SERIES
K933850 PHILIPS 45 SERIES
Search all 20 clearances from Philips Hearing Instruments Co. →