Last synced on 14 November 2025 at 11:06 pm

ULTRAPROBE

Page Type
Cleared 510(K)
510(k) Number
K810133
510(k) Type
Traditional
Applicant
ARS MAGNA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1981
Days to Decision
141 days

ULTRAPROBE

Page Type
Cleared 510(K)
510(k) Number
K810133
510(k) Type
Traditional
Applicant
ARS MAGNA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1981
Days to Decision
141 days