Last synced on 25 January 2026 at 3:41 am

BIOPSY KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892389
510(k) Type
Traditional
Applicant
I M, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
7/17/1989
Days to Decision
101 days

BIOPSY KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892389
510(k) Type
Traditional
Applicant
I M, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
7/17/1989
Days to Decision
101 days