Last synced on 2 December 2022 at 11:04 pm

LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893723
510(k) Type
Traditional
Applicant
LORI MEDICAL LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1989
Days to Decision
114 days