3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031
FDA 510(k) clearance K860313 · decided 1986-03-17
Clearance details
- K-number
- K860313
- Device name
- 3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031
- Applicant
- Johnson & Johnson Professionals, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-01-28
- Decision date
- 1986-03-17
- Days to decision
- 48 days
- Clearance type
- Traditional
- Product code
- HGL
- Device class
- 2
- Regulation number
- 884.2960
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Ramsey, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.