Last synced on 14 November 2025 at 11:06 pm

ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K950255
510(k) Type
Traditional
Applicant
ARGUS MEDICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1995
Days to Decision
213 days
Submission Type
Statement

ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K950255
510(k) Type
Traditional
Applicant
ARGUS MEDICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1995
Days to Decision
213 days
Submission Type
Statement