AUTONOM
FDA 510(k) clearance K780312 · decided 1978-04-05
Clearance details
- K-number
- K780312
- Device name
- AUTONOM
- Applicant
- Autonomic Equipment Supply Co,
- Decision
- Substantially Equivalent
- Date received
- 1978-02-15
- Decision date
- 1978-04-05
- Days to decision
- 49 days
- Clearance type
- Traditional
- Product code
- KNM
- Device class
- 1
- Regulation number
- 890.5765
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| AUTONORM & NERV-A-NORM (K811956) | Autonomic Equipment Supply Co, | 1981-07-31 |
Recalls involving this device
No recalls on record reference this clearance.