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CODE #D2020-FINE NEEDLE ASPIRATION BIOPSY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882105
510(k) Type
Traditional
Applicant
DIANON SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
7/11/1988
Days to Decision
53 days

CODE #D2020-FINE NEEDLE ASPIRATION BIOPSY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882105
510(k) Type
Traditional
Applicant
DIANON SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
7/11/1988
Days to Decision
53 days