510(k) K935160
- Device
- MINIMUFFS
- Applicant
- NATUS MEDICAL, INC.
- 510(k) number
- K935160
- Product code
- EWE
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1995-02-09
- Date received
- 1993-10-29
- Regulation
- 510(k) Premarket Notification
- Classification name
- Protector, Hearing (circumaural)
- Medical specialty
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Review panel
- Ear Nose & Throat
- Device class
- U
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- LISA TAYLOR
- Address
- 1501 Industrial Rd. San Carlos CA US 94070 94070
FDA Registration Numbers#
- 3006698500
- 1930027
- 3042251637
- 3025759181
- 3006621348
- 3016769292
- 8022210
- 3006450239
- 3030536686
- 3017067322
- 3013152643
- 3015601315
- 3012903018
- 3003627840
- 3038613785
- 3013598746
- 3009845346
- 3002661124
- 3006713791
- 3014144373
Source Documents#
Legacy Summary#
summary
FDA Review#
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