Vcs Doppler Transceiver, Model 09-0023-01

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K052209 ↗

FDA Product Code

DPW

Device Class

Class II

Regulation

21 CFR Part 870.2100

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Vcs-A Series Clamp

  Class II

  FDA 510(k) K011863 Active Cleared 15 Feb 2002

• Transvaginal Doppler Probe

  Class II

  FDA 510(k) K031358 Active Cleared 9 May 2003

• Transvaginal Doppler Probe, Model 09-0006-02

  Class II

  FDA 510(k) K023024 Active Cleared 26 Sep 2002

• Burbank Tenaculum

  Class II

  FDA 510(k) K060573 Active Cleared 21 Apr 2006

• Vcs-A Series Clamp with Doppler Ultrasound, Model 09-0007-01 and 09-0007-02

  Class II

  FDA 510(k) K023154 Active Cleared 20 Dec 2002

• Transvaginal Doppler Clamp, Models: 09-0016-01, 09-0016-02, 09-0016-03

  Class II

  FDA 510(k) K031812 Active Cleared 12 Dec 2003

See all devices from Vascular Control Systems, Inc. →