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Argosy Intl. (USA), Inc.

Mchenry, IL, US

Argosy Intl. (Usa), Inc. appears in FDA device records in Mchenry, IL. FDA records list 14 510(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
14
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 14 510(k) clearances for Argosy Intl. (USA), Inc. between 1978 and 1982. The busiest year on record is 1978, with 12. The most recent is 1982, with 1.

Clearances by year, as a table
510(k) clearance decisions for Argosy Intl. (USA), Inc., by decision year
YearClearances
197812
19791
19821
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K823075REXTONSubstantially Equivalent
K791548REXTON HS(HEARING SYSTEM)HSDSubstantially Equivalent
K781096HEARING AID, EYEGLASS, B-12ESDSubstantially Equivalent
K781095HEARING AID, BEHIND THE EARESDSubstantially Equivalent
K781094HEARING AID, EYEGLASSESDSubstantially Equivalent
K780922UM VII (BEHIND THE EAR)ESDSubstantially Equivalent
K780921MM-CE DM (BEHIND THE EAR)ESDSubstantially Equivalent
K780920MM-CE 11 (BEHIND THE EAR)ESDSubstantially Equivalent
K780919M25 PP (BEHIND THE EAR)ESDSubstantially Equivalent
K780918PRIMO CEDM (BEHIND THE EAR)ESDSubstantially Equivalent
K780917PRIMO CE (BEHIND THE EAR)ESDSubstantially Equivalent
K780916780 UE (BEHIND THE EAR)ESDSubstantially Equivalent
K780915780 SE (BEHIND THE EAR)ESDSubstantially Equivalent
K780914PM 25 PP (BODY AID)ESDSubstantially 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