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Alexon, Inc.

Mountain View, CA, US

Alexon, Inc. appears in FDA device records in Mountain View, CA. FDA records list 10 510(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
10
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 10 510(k) clearances for Alexon, Inc. between 1991 and 1994. The busiest year on record is 1992, with 5. The most recent is 1994, with 2.

Clearances by year, as a table
510(k) clearance decisions for Alexon, Inc., by decision year
YearClearances
19911
19925
19932
19942
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K934493PROSPECT MICROPLATE ASSAYLLHSubstantially Equivalent
K942098PROSPECT GIARDIAMHISubstantially Equivalent
K931147PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATIONMHISubstantially Equivalent
K930451PROSPEC T GIARDIA MICROTITER ASSAYMHISubstantially Equivalent
K922675PROSPECT GIARDIA CONTROLSMHISubstantially Equivalent
K922010PROSPECT(TM) GIARDIA MICROTITER ASSAY/MODIFICATIONMHISubstantially Equivalent
K920817MODIFICATION PROSPECT GIARDIA RAPID ASSAYMHISubstantially Equivalent
K912242PROSPECT(TM/CRYPTOSPORIDIUMMHJSubstantially Equivalent
K915093PROSPECT(TM) GIARDIA RAPID ASSAYMHISubstantially Equivalent
K911337PROSPEC T/GIARDIA RAPID ASSAYMHISubstantially 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