Medical Device Manufacturer · US , New York , NY

Konica Medical Corp. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1990

Total

Cleared

Denied

Konica Medical Corp. has 12 FDA 510(k) cleared radiology devices. Based in New York, US.

Historical record: 12 cleared submissions from 1990 to 1999.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Konica Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Konica Medical Corp.

12 devices

1-12 of 12

Cleared Jun 18, 1999

KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSOR

KONICA SRX-501A AUTOMATIC X-RAY FILM PROCESSOR

K931315 · IXW

Radiology · 274d

Cleared Dec 14, 1993

KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSOR

K931316 · IXW

Radiology · 274d

Cleared Dec 14, 1993

KONICA SRX-301 AUTOMATIC X-RAY FILM PROCESSOR

K931317 · IXW

Radiology · 274d

Cleared Dec 14, 1993

KONICA LD-4500 LASER DIGITIZER

K933830 · LMA

Radiology · 131d

Cleared Sep 07, 1993

KONICA SRX-101 AUTOMATIC X-RAY FILM PROCESSOR

K931312 · IXW

Radiology · 176d

Cleared Sep 07, 1993

KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR

K931313 · IXW

Radiology · 176d

Cleared Sep 07, 1993

KONICA QX-70 AUTOMATIC X-RAY FILM PROCESSOR

Konica Medical Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Konica Medical Corp.

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