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ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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