PK2025/PK2045 Programmable Video Controller

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K893644 ↗

FDA Product Code

JAA

Device Class

Class II

Regulation

21 CFR Part 892.1650

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Grundig Electronics Various Models

  Class II

  FDA 510(k) K915232 Active Cleared 9 Jan 1992

• Cine Camera Control Model PK2037

  Class II

  FDA 510(k) K896615 Active Cleared 4 Jan 1990

• Display Processor - Model IDP5100

  Class II

  FDA 510(k) K920550 Active Cleared 13 Apr 1992

• 1 Video Tape Recorder Model Bk-224 H

  Class II

  FDA 510(k) K892934 Active Cleared 20 Jul 1989

• Philips RT250 Collimator (PK8050)

  Class II

  FDA 510(k) K885126 Active Cleared 1 Jun 1989

• Video Annotator Model PK2310

  Class II

  FDA 510(k) K910384 Active Cleared 16 Apr 1991

See all devices from Perkins Mfg. Co. →