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Imaging Dynamics Company, Ltd.

Calgary, CA

Imaging Dynamics Company , Ltd. appears in FDA device records in Calgary, CA. FDA records list 21 510(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
21
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 21 510(k) clearances for Imaging Dynamics Company, Ltd. between 2000 and 2017. The busiest year on record is 2006, with 8. The most recent is 2017, with 4.

Clearances by year, as a table
510(k) clearance decisions for Imaging Dynamics Company, Ltd., by decision year
YearClearances
20001
20041
20068
20076
20111
20174
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K173273Aquarius 8600 1417WCI; Aquarius 8600 1717WCIMQBSubstantially Equivalent
K171169Aquarius 8600 1417TG and Aquarius 8600 1717TGMQBSubstantially Equivalent
K171175Aquarius 8600 1417WCMQBSubstantially Equivalent
K170202Aquarius 8600MQBSubstantially Equivalent
K111098INNOVAXION FP, INNOVAXION FP 1600 PLUS, MAGELLANMQBSubstantially Equivalent
K071401X3C 2200 DIGITAL RADIOGRAPHIC SYSTEMKPRSubstantially Equivalent
K071408X3C 1100 RADIOGRAPHIC TABLE WITH DIGITAL RADIOGRAPHIC DETECTORKPRSubstantially Equivalent
K071403X3C 1600 DIGITAL RADIOGRAPHIC SYSTEMKPRSubstantially Equivalent
K071409X3C 1590 DIGITAL RADIOGRAPHIC SYSTEMKPRSubstantially Equivalent
K071402X3C 1600 PLUS DIGITAL RADIOGRAPHIC SYSTEMKPRSubstantially Equivalent
K070079X3C DIGITAL RADIOGRAPHIC DETECTORMQBSubstantially Equivalent
K063247XPLORER 1800 DIGITAL RADIOGRAPHIC SYSTEM WITH UNIVERSAL STANDKPRSubstantially Equivalent
K063246XPLORER 1500 DIGITAL RADIOGRAPHIC SYSTEM WITH STANDKPRSubstantially Equivalent
K063039XPLORER 2200 DIGITAL RADIOGRAPHIC SYSTEMMQBSubstantially Equivalent
K062634ORTHOXPKPRSubstantially Equivalent
K062586XPLORER 1600 PLUSMQBSubstantially Equivalent
K062417XPLORER 1100KPRSubstantially Equivalent
K062405XPLORER 1590KPRSubstantially Equivalent
K061595XAMINERKPRSubstantially Equivalent
K042041XPLORER 1600MQBSubstantially Equivalent
K992955XPLORER 1000MQBSubstantially 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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What MDM checks, and what it does not

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