FDA 510(k)
FDA class 1
Substantially Equivalent
🇨🇦 Canada
OVATION HDP
K Number: K972373
·
Decision Jul 29, 1997
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
6
Review Days
34
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Basic Information
- Device Name
- OVATION HDP
- K Number
- K972373
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.3300
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Orsonique, Inc.
- Date Received
- June 25, 1997
- Decision Date
- July 29, 1997
- Product Code
- ESD
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| ESD | Hearing Aid, Air-Conduction, Prescription | FDA class 1 | Ear, Nose, Throat |
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Other Clearances by Orsonique, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K963819 | OVATION ASP | Oct 28, 1996 | Substantially Equivalent |
| K963818 | OVATION AGC-2 | Oct 28, 1996 | Substantially Equivalent |
| K963820 | OVATION LINEAR | Oct 28, 1996 | Substantially Equivalent |
| K963822 | OVATION AGC-3 | Oct 28, 1996 | Substantially Equivalent |
| K963821 | OVATION AGC-1 | Oct 28, 1996 | Substantially Equivalent |