FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AUTONORM & NERV-A-NORM
K Number: K811956
·
Decision Jul 31, 1981
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
1
Applicant Total
2
Review Days
22
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Basic Information
- Device Name
- AUTONORM & NERV-A-NORM
- K Number
- K811956
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.5765
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Autonomic Equipment Supply Co,
- Date Received
- July 9, 1981
- Decision Date
- July 31, 1981
- Product Code
- KNM
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| KNM | Device, Pressure Applying | FDA class 1 | Physical Medicine |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KNM), ordered by most recent decision date.
View allOther Clearances by Autonomic Equipment Supply Co,
| K Number | Device Name | ||
|---|---|---|---|
| K780312 | AUTONOM | Apr 5, 1978 | Substantially Equivalent |