Last synced on 14 November 2025 at 11:06 pm

RECORDER DMI

Page Type
Cleared 510(K)
510(k) Number
K830489
510(k) Type
Traditional
Applicant
DIAGNOSTIC MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1983
Days to Decision
99 days

RECORDER DMI

Page Type
Cleared 510(K)
510(k) Number
K830489
510(k) Type
Traditional
Applicant
DIAGNOSTIC MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1983
Days to Decision
99 days