ADR ULTRASOUND MODEL 4000 L
FDA 510(k) clearance K828050 · decided 1982-09-29
Clearance details
- K-number
- K828050
- Device name
- ADR ULTRASOUND MODEL 4000 L
- Applicant
- Adr Ultrasound
- Decision
- Substantially Equivalent
- Date received
- 1982-08-31
- Decision date
- 1982-09-29
- Days to decision
- 29 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Tempe, AZ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.