Mid-500

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K940117 ↗

FDA Product Code

MEB

Device Class

Class II

Regulation

21 CFR Part 880.5725

Advisory Committee

General Hospital

FDA Decision

ST

• Verifuse Ambulatory Pump

  Class II

  FDA 510(k) K934551 Active Cleared 17 Mar 1994

• Homepump (Disp. Elastomeric Infusion Device)

  Class II

  FDA 510(k) K896546 Active Cleared 6 Feb 1990

• Chemo Priming Pin

  Class II

  FDA 510(k) K914924 Active Cleared 6 Mar 1992

• Homepump NSF

  Class II

  FDA 510(k) K932740 Active Cleared 6 Oct 1993

• Auto Sash (Tm)

  Class II

  FDA 510(k) K910695 Active Cleared 21 Mar 1991

• C-Series Homepump

  Class II

  FDA 510(k) K944692 Active Cleared 2 May 1995

See all devices from Block Medical, Inc. →