LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT— 510(k) K893723
Substantially EquivalentLori Medical Laboratories, Inc.
FDA 510(k) clearance K893723 for LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT, Substantially Equivalent on 1989-09-08. Applicant: Lori Medical Laboratories, Inc..
Clearance details
- Applicant
- Lori Medical Laboratories, Inc.
- Product code
- Code ESD
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Long Lake, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.