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

SIEMENS SILICONE IMPRESSION MATERIAL

K Number: K872152 · Decision Aug 11, 1987
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
42
Review Days
68

Basic Information

Device Name
SIEMENS SILICONE IMPRESSION MATERIAL
K Number
K872152
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
SIEMENS HEARING INSTRUMENTS, INC.
Date Received
June 4, 1987
Decision Date
August 11, 1987
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 SIEMENS HEARING INSTRUMENTS, INC.

K Number Device Name
K071462 UNITY 2 HIA & PROBE ( FOR USE WITH UNITY 2)
K011364 CUSTOM TCI (TINNITUS CONTROL INSTRUMENT)
K011366 CUSTOM TCI-COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)
K003559 TCI (TINNITUS CONTROL INSTRUMENT)
K003558 TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)
K972998 PRISMA
K962170 SIEMENS VITA 160 SERIES POCKET HEARING INSTRUMENT: VITA 162E,166M,168PP
K952940 PERSONAL PROGRAMMER 2000
K951828 FULL DYNAMIC RANGE COMPRESSION BEHIND THE EAR HEARING INSTRUMENT
K952263 PROGRAMMABLE TWO MEMORY, SINGLE BAND BEHIND THE EAR HEARING INSTRUMENT
Search all 42 clearances from SIEMENS HEARING INSTRUMENTS, INC. →