QUINTREX 0515 PROGRAMMABLE PULSE GEN.
FDA 510(k) clearance K802223 · decided 1980-09-12
Clearance details
- K-number
- K802223
- Device name
- QUINTREX 0515 PROGRAMMABLE PULSE GEN.
- Applicant
- Medcor, Inc.
- Decision
- Unknown
- Date received
- 1980-09-12
- Decision date
- 1980-09-12
- Days to decision
- 0 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.