Last synced on 20 June 2025 at 11:06 pm

Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223300
510(k) Type
Traditional
Applicant
GEOTEK Medikal Ltd sti
Country
Turkey
FDA Decision
Substantially Equivalent
Decision Date
4/21/2023
Days to Decision
176 days
Submission Type
Statement

Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223300
510(k) Type
Traditional
Applicant
GEOTEK Medikal Ltd sti
Country
Turkey
FDA Decision
Substantially Equivalent
Decision Date
4/21/2023
Days to Decision
176 days
Submission Type
Statement