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In-Line Diagnostics Corp.

Kaysville, UT, US

In-Line Diagnostics Corp. appears in FDA device records in Kaysville, UT. FDA records list 8 510(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
8
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 8 510(k) clearances for In-Line Diagnostics Corp. between 1995 and 2000. The busiest year on record is 1995, with 2. The most recent is 2000, with 1.

Clearances by year, as a table
510(k) clearance decisions for In-Line Diagnostics Corp., by decision year
YearClearances
19952
19961
19971
19981
19992
20001
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K001763CRIT-LINE MONITOR III (CLM III)MQSSubstantially Equivalent
K992227CRIT-LINE MONITOR III (CLM III)MQSSubstantially Equivalent
K983551CRIT-SCAN II MONITORGKFSubstantially Equivalent
K982412MODIFICATION OF CRIT-LINE MONITOR III (CLM III)MQSSubstantially Equivalent
K972470CRIT-LINE MONITOR (CLMIII)MQSSubstantially Equivalent
K953875CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)MQSSubstantially Equivalent
K950942CRIT-LINE HEMATOCRIT ALERTJPISubstantially Equivalent
K935958CRIT-LINE BLOOD CHAMBER WITH E-BEAMKOCSubstantially 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