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Maxtec, LLC

Salt Lake City, UT, US

Maxtec, LLC appears in FDA device records in Salt Lake City, UT. 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 Maxtec, LLC between 2004 and 2023. The busiest year on record is 2016, with 2. The most recent is 2023, with 2.

Clearances by year, as a table
510(k) clearance decisions for Maxtec, LLC, by decision year
YearClearances
20041
20071
20111
20121
20141
20162
20191
20232
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K231895Maxtec MaxBlend2+pBZRSubstantially Equivalent
K221734Maxtec MaxO2 ME+pCCLSubstantially Equivalent
K182362MaxCap Ped and MaxCap NeoCCKSubstantially Equivalent
K161718MaxBlend 2, MaxBlend LiteBZRSubstantially Equivalent
K153659MaxO2MECCLSubstantially Equivalent
K133540FLOCAPCCKSubstantially Equivalent
K113232MAXMIXING BLOCKBZRSubstantially Equivalent
K112402ULTRAMAXO2 OXYGEN ANALYERCCLSubstantially Equivalent
K063488MAXO2 CUCCLSubstantially Equivalent
K040484MAXO2+, MODEL A AND AECCLSubstantially 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