SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT
FDA 510(k) clearance K973176 · decided 1997-11-21
Clearance details
- K-number
- K973176
- Device name
- SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT
- Applicant
- Lotus Technologies
- Decision
- Unknown
- Date received
- 1997-08-25
- Decision date
- 1997-11-21
- Days to decision
- 88 days
- Clearance type
- Traditional
- Product code
- KGA
- Advisory committee
- Unknown
- Location
- Austin, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.