MORTARA INSTRUMENT ODEL ELI 50I
FDA 510(k) clearance K915730 · decided 1992-11-10
Clearance details
- K-number
- K915730
- Device name
- MORTARA INSTRUMENT ODEL ELI 50I
- Applicant
- Mortara Instrument, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-12-20
- Decision date
- 1992-11-10
- Days to decision
- 326 days
- Clearance type
- Traditional
- Product code
- LOS
- Advisory committee
- Unknown
- Location
- Milwaukee, WI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.