FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RION AUDIOMETER AA-67

K Number: K812951 · Decision Nov 6, 1981
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
41
Applicant Total
51
Review Days
16

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Basic Information

Device Name
RION AUDIOMETER AA-67
K Number
K812951
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Rion Acoustic Instruments, Inc.
Date Received
October 21, 1981
Decision Date
November 6, 1981
Product Code
GWO
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWO Plate, Cranioplasty, Preformed, Alterable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWO), ordered by most recent decision date.

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Other Clearances by Rion Acoustic Instruments, Inc.

K Number Device Name
K874510 RIONET HEARING AID HB-75
K862670 RIONET HEARING AID HB-35PT
K861728 RIONET HEARING AID
K853637 RIONET HEARING AID HI-07
K853636 RIONET HEARING AID HI-06
K853638 RIONET HEARING AID
K852453 RIONET HEARING AID HB-69HT
K852452 RIONET HEARING AID HB-71P
K852451 RIONET HEARING AID HB-34HT
K844059 RIONET HEARING AID HB-34AS
Search all 51 clearances from Rion Acoustic Instruments, Inc. →