FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SILENT NIGHT II
K Number: K981034
·
Decision Oct 30, 1998
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
2
Review Days
225
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Basic Information
- Device Name
- SILENT NIGHT II
- K Number
- K981034
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.2375
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Sleep Solutions, Inc.
- Date Received
- March 19, 1998
- Decision Date
- October 30, 1998
- Product Code
- MNR
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| MNR | Ventilatory Effort Recorder | FDA class 2 | Anesthesiology |
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Other Clearances by Sleep Solutions, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K000253 | SILENT NIGHT V | Nov 16, 2000 | Substantially Equivalent |