ClearanceBrief
Company ยท US

Vidco, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1997. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXJDisplay, Cathode-Ray Tube, Medical5
MSXSystem, Network And Communication, Physiological Monitors2
DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 22, 1997K972880MDP2000 MEDICAL DATA PROCESSOR
Vidco, Inc.
MSX
Aug 18, 1994K934093580CDR DISPLAY DRIVER
Vidco, Inc.
DXJ
Jun 20, 1994K932894620CSR DISPLAY DRIVER
Vidco, Inc.
DXJ
May 4, 1994K926298520 DISPLAY DRIVER- STATUS I
Vidco, Inc.
DRT
Dec 16, 1993K926219516YT DISPLAY DRIVER
Vidco, Inc.
DXJ
Nov 8, 1993K926162580CD DISPLAY DRIVER
Vidco, Inc.
DXJ
Mar 2, 1989K890353SMDS460 SURGICAL MONITOR DISPLAY SYSTEM
Vidco, Inc.
DXJ

Latest recalls

DateFirm and productCodeLinked 510(k)
Jan 4, 2016Vidco, Inc.
Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3, or PGM340R4. The MDP2000 is intended for use in conjunction with patient monitoring equipment. The MDP2000 is
Terminated
MSXK972880
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