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Midwest City Hearing Aid Center

Midwest City, OK, US

Midwest City Hearing Aid Center appears in FDA device records in Midwest City, OK. FDA records list 12 510(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
12
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 12 510(k) clearances for Midwest City Hearing Aid Center between 1995 and 1997. The busiest year on record is 1995, with 9. The most recent is 1997, with 1.

Clearances by year, as a table
510(k) clearance decisions for Midwest City Hearing Aid Center, by decision year
YearClearances
19959
19962
19971
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K970430ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCIESDSubstantially Equivalent
K963604DYNAMIC EQ II - 2 CHANNEL WIDE DYNAMIC RANGE COMPRESSIONESDSubstantially Equivalent
K963607HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANALESDSubstantially Equivalent
K953729K AMP FULL SHELL AND IN THE EARESDSubstantially Equivalent
K953728RX12 LINEAR FULL SHELL AND IN THE CANALESDSubstantially Equivalent
K953631SNIP INPUT COMPRESSION CLASS AESDSubstantially Equivalent
K952986SPI-SECRET PERSONAL INSTRUMENT CICESDSubstantially Equivalent
K953038DYNAMIC EQ/CLASS DESDSubstantially Equivalent
K953036DB PUSH-PULL HEARING AIDESDSubstantially Equivalent
K952821MWCHAC 95 FS 12345ESDSubstantially Equivalent
K952820MWCHAC 95 C 12345ESDSubstantially Equivalent
K953037CUSTOM CANAL & FULL CONCHA INSTR (CLASS D CIR OPT)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