FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER

K Number: K033108 · Decision Oct 27, 2003
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
5
Review Days
27

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER
K Number
K033108
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vivosonic, Inc.
Date Received
September 30, 2003
Decision Date
October 27, 2003
Product Code
EWO
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
EWO Audiometer

Similar 510(k) Clearances

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

View all

Other Clearances by Vivosonic, Inc.

K Number Device Name
K242954 Integrity V500 (Integrity, Integrity with VEMP)
K080060 VIVOSONIC NEUROSCREEN
K043396 INTEGRITY, MODEL V500
K003364 VIVO 200 DPS VIVOSCAN