Last synced on 14 November 2025 at 11:06 pm

T19S BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K902077
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1990
Days to Decision
80 days

T19S BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K902077
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1990
Days to Decision
80 days