510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Vidar Systems Corp.

Herndon, VA, US

Vidar Systems Corp. appears in FDA device records in Herndon, VA. FDA records list 13 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
13
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 13 510(k) clearances for Vidar Systems Corp. between 1993 and 2013. The busiest year on record is 2000, with 2. The most recent is 2013, with 2.

Clearances by year, as a table
510(k) clearance decisions for Vidar Systems Corp., by decision year
YearClearances
19931
19981
19991
20002
20011
20031
20072
20102
20132
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDLMASubstantially Equivalent
K130406DIAGNOSTICPRO EDGELMASubstantially Equivalent
K102476TELERADPROLMASubstantially Equivalent
K093809VIDAR DENTAL FILM DIGITIZERLMASubstantially Equivalent
K071193VIDAR VISION 3000 AND 4000 X-RAY SYSTEMSMQBSubstantially Equivalent
K070563VIDAR VISION 2000MQBSubstantially Equivalent
K024171VIDAR BONE TRACK SYSTEM SOFTWAREJAKSubstantially Equivalent
K011049EXPRESSSUITELMASubstantially Equivalent
K993598MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205LMASubstantially Equivalent
K993599DIAGNOSTIC PRO, MODEL 12772, VXR-16, MODEL 13020, VXR-16 DOSIMETRY PRO, MODEL 13019LMASubstantially Equivalent
K993597PLLL, TELERADPRO, MODEL 12714/12715, VXR-12 PLUS, MODEL 8619/9617LMASubstantially Equivalent
K974315VIDAR VXR LS LASER FILM DIGITIZERLMASubstantially Equivalent
K933632MEDSCAN 12LMASubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain