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Konica Medical Corp.

New York, NY, US

Konica Medical Corp. appears in FDA device records in New York, NY. 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 Konica Medical Corp. between 1990 and 1999. The busiest year on record is 1993, with 7. The most recent is 1999, with 1.

Clearances by year, as a table
510(k) clearance decisions for Konica Medical Corp., by decision year
YearClearances
19901
19937
19961
19972
19991
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K990969KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K963914CM & CM DS-7IXASubstantially Equivalent
K963913MD100 & MM150EAMSubstantially Equivalent
K955583VIFSJAKSubstantially Equivalent
K933830KONICA LD-4500 LASER DIGITIZERLMASubstantially Equivalent
K931317KONICA SRX-301 AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K931316KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K931315KONICA SRX-501A AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K931314KONICA QX-70 AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K931313KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K931312KONICA SRX-101 AUTOMATIC X-RAY FILM PROCESSORIXWSubstantially Equivalent
K896739KONICA KFDR-SLMASubstantially 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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What MDM checks, and what it does not

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Data as of , FDA export datePage updated Source: openFDA, public domain