Biopsy Guide Attachment for Use with Fetascan 2000 and 2000A

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K827375 ↗

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Fetascan 1000, 1000A Obstetrical Data

  Class II

  FDA 510(k) K813458 Active Cleared 28 Jan 1982

• Entrekin Model Dx-300 Continuous Wave Ultrasonic Doppler Transducer

  Not classified

  FDA 510(k) K828586 Active Cleared 14 Dec 1982

• Biopsy Guide Attachment for Use with Fetascan 800

  Not classified

  FDA 510(k) K827376 Active Cleared 2 Jul 1982

• Medical Labs Fetal Scan #1000 W/Central

  Class II

  FDA 510(k) K822830 Active Cleared 30 Sep 1982

• Fetascan 2000, 2000A Obstetrical Data

  Class II

  FDA 510(k) K813457 Active Cleared 12 Feb 1982