ClearanceBrief
Company ยท US

Vasomedical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2011. Name variants (Inc, Corp, punctuation) are merged.

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

Product codes

CodeDeviceRecords
DSHRecorder, Magnetic Tape, Medical4
DRNDevice, Counter-Pulsating, External3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 28, 2011K111180VASOMEDICAL-BIOX 12- CHANNEL AMBULATORY ECG HOLTER RECORDER MODEL 1304, VASOMEDICAL-BIOX 3- CHANNEL MINIATURE AMBULATORY
Vasomedical, Inc.
DSH
Jun 24, 2011K111096VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE RECORDER MODEL 2302, VASOMEDICAL-BIOX AMBULATORY
Vasomedical, Inc.
DSH
Apr 2, 2010K092785COMBINED VASOMEDICAL-BIOX AMBULATORY ECG & BLOOD PRESSURE RECORDER & ANALYSIS SOFTWARE, 2301
Vasomedical, Inc.
DSH
Apr 1, 2009K083820VASOMEDICAL BIOX CB-1305-C, 3 CHANNEL ECG HOLTER MONITOR, MODEL CB-1305-C
Vasomedical, Inc.
DSH
Mar 1, 2004K033617EECP THERAPY SYSTEM MODEL TS4 WITH/WITHOUT PLUSE OXIMETRY
Vasomedical, Inc.
DRN
Jun 14, 2002K020857EECP THERAPY SYSTEM MODEL TS3 WITH PULSE OXIMETRY AND ENHANCED EXTERNAL COUNTERPULSATION EECP MC-2 EXTERNAL COUNTER
Vasomedical, Inc.
DRN
Dec 6, 2000K003469EECP THERAPY SYSTEM, MODEL TS3
Vasomedical, Inc.
DRN

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes