MINI NICHOLES
FDA 510(k) clearance K812098 · decided 1981-08-18
Clearance details
- K-number
- K812098
- Device name
- MINI NICHOLES
- Applicant
- Healthcare Ind.
- Decision
- Substantially Equivalent
- Date received
- 1981-07-24
- Decision date
- 1981-08-18
- Days to decision
- 25 days
- Clearance type
- Traditional
- Product code
- CAH
- Device class
- 2
- Regulation number
- 868.5260
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.