HF MEGA EAR— 510(k) K960567
Substantially EquivalentMaxi-Aids, Inc.
FDA 510(k) clearance K960567 for HF MEGA EAR, Substantially Equivalent on 1996-10-16. Applicant: Maxi-Aids, Inc.. Device class: 2.
Clearance details
- Applicant
- Maxi-Aids, Inc.
- Product code
- Code EPF
- Device class
- Class 2
- Regulation
- 21 CFR 874.3320
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Farmingdale, NY, US
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