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No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K910695 ↗

FDA Product Code

FPA

Device Class

Class II

Regulation

21 CFR Part 880.5440

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• 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

• C-Series Homepump

  Class II

  FDA 510(k) K944692 Active Cleared 2 May 1995

• Mid-500

  Class II

  FDA 510(k) K940117 Active Cleared 10 Jun 1994

See all devices from Block Medical, Inc. →