Last synced on 16 February 2024 at 11:04 pm

MRP-5000 AND 7000 BILATERAL/UNILATERAL TMJ COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923140
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/1992
Days to Decision
178 days
Submission Type
Summary