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

Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App (iOS) (P1646054); Baha Smart App (Android) (P1646035); Baha SoundBand

K Number: K250215 · Decision May 29, 2025
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
50
Applicant Total
3
Review Days
125

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Basic Information

Device Name
Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App (iOS) (P1646054); Baha Smart App (Android) (P1646035); Baha SoundBand
K Number
K250215
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3302
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cochlear
Date Received
January 24, 2025
Decision Date
May 29, 2025
Product Code
LXB
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
LXB Hearing Aid, Bone Conduction

Similar 510(k) Clearances

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

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Other Clearances by Cochlear

K Number Device Name
K231204 Cochlear™ Osia® System; Cochlear™ Osia® OSI300 Implant; Cochlear™ Magnet Cassette; Cochlear™ Non-Magnetic Cassette; Cochlear™ Osia® 2(I) Sound Processor; Cochlear™ Osia® Fitting Software 2; Cochlear™ Osia® Smart App
K223672 Instrument Case P1340904