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Schiller America, Inc.

Tustin, CA, US

Schiller America, Inc. appears in FDA device records in Tustin, 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 Schiller America, Inc. between 1990 and 1998. The busiest year on record is 1995, with 4. The most recent is 1998, with 2.

Clearances by year, as a table
510(k) clearance decisions for Schiller America, Inc., by decision year
YearClearances
19902
19921
19954
19971
19982
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K973751MT-200DQKSubstantially Equivalent
K973735MICROVIT MT-100DSHSubstantially Equivalent
K970879CARDIOVIT CS-200LOSSubstantially Equivalent
K953396CARDIOVIT AT-1C, AT-2CLOSSubstantially Equivalent
K954066MINISCOPE MS-3DPSSubstantially Equivalent
K941462CARDIOVIT AT-5CLOSSubstantially Equivalent
K946205CARDIOVIT AT-1, P-80DPSSubstantially Equivalent
K914970CARDIOVIT CS-100LOSSubstantially Equivalent
K896121SCHILLER MODEL SP-200 SPIROVIT(TM)BZGSubstantially Equivalent
K896120SCHILLER MODEL SP-100 SPIROVIT(TM)BZGSubstantially 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