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

ARGOSY DYNAMEQ

K Number: K971699 · Decision Jul 3, 1997
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
24
Review Days
56

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Basic Information

Device Name
ARGOSY DYNAMEQ
K Number
K971699
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
Argosy Electronics
Date Received
May 8, 1997
Decision Date
July 3, 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 Argosy Electronics

K Number Device Name
K974242 ARGOSY PROGRAMMABLE ONQUE
K961729 ARGOSY PROGRAMMABLE
K954038 K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENT
K952452 OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL
K952451 CLASS D LINEAR WITH ACTIVE TONE CONTROL
K952450 WIDE DYNAMIC RANGE COMPRESSION WITH ACTIVE TONE CONTROL
K952454 EXPANDER WITH ACTIVE TONE CONTROL
K952455 IMPROVED MANHATTAN II
K952453 INPUT COMPRSSION LIMITER WITH ACTIVE TONE CONTROL
K944078 PROGRAM 3-CH SER HEAR AIDS W/PROGRAM FIT SYST/PRO FIT
Search all 24 clearances from Argosy Electronics →