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

PERFECT EAR/ MINI-CANAL/ PE-M, PE-ML, PE-MD), PERFECT EAR/ C.I.C./ (PEC, PE-CD) (WITH OR WITHOUT RID-WAX BARRIER)

K Number: K973972 · Decision Nov 4, 1997
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
3
Review Days
15

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Basic Information

Device Name
PERFECT EAR/ MINI-CANAL/ PE-M, PE-ML, PE-MD), PERFECT EAR/ C.I.C./ (PEC, PE-CD) (WITH OR WITHOUT RID-WAX BARRIER)
K Number
K973972
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
Perfect Ear
Date Received
October 20, 1997
Decision Date
November 4, 1997
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 Perfect Ear

K Number Device Name
K960410 PERFECT EAR PE/PE-AGC/PE-B/PE-PWR
K931984 PERFECT EAR/PE