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Kmi Kolster Methods, Inc.

Anaheim, CA, US

Kmi Kolster Methods, Inc. appears in FDA device records in Anaheim, CA. FDA records list 6 510(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
6
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 6 510(k) clearances for Kmi Kolster Methods, Inc. between 1999 and 2006. The busiest year on record is 2001, with 2. The most recent is 2006, with 1.

Clearances by year, as a table
510(k) clearance decisions for Kmi Kolster Methods, Inc., by decision year
YearClearances
19991
20001
20012
20051
20061
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K060414KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTUREGAWSubstantially Equivalent
K043591FEATHERLIFT EXTENDED APTOS THREADGAWSubstantially Equivalent
K012236STARS2000 POWER CANNULAQPBSubstantially Equivalent
K010702XUB EXTERNAL ULTRASOUNDIMISubstantially Equivalent
K002859SSW-STERILE SOLUTION WARMERLHCSubstantially Equivalent
K991203IRRIGATION OR INFUSION PUMP K PUMPFRNSubstantially 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