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INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892376
510(k) Type
Traditional
Applicant
CONCEPT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1989
Days to Decision
118 days

INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892376
510(k) Type
Traditional
Applicant
CONCEPT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1989
Days to Decision
118 days