Medical Device Manufacturer · US , Mchenry , IL

Vxtra Corp. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1980

Total

Cleared

Denied

Vxtra Corp. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1980 to 1983. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Vxtra Corp. Filter by specialty or product code using the sidebar.

Vxtra 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 - Vxtra Corp.

10 devices

1-10 of 10

Cleared Oct 19, 1983

OCUTOME PARATUBING SET

IRRIGATION/ASPIRATION KIT

K830385 · HQC

Ophthalmic · 60d

Cleared Oct 19, 1981

ADJUSTABLE MICROSURGICAL KNIFE

General & Plastic Surgery · 14d

Cleared Aug 31, 1981

MICROSURGICAL BLADE

K812160 · GES

General & Plastic Surgery · 33d

Cleared Apr 21, 1980

DISPOSABLE PRE-GELLED ELECTROSURGICAL

K800557 · GEI

General & Plastic Surgery · 40d

Cleared Feb 22, 1980

VXTRA BACK PACK EKG ELECTRODE CAT. NO.

K792436 · DRX

Cardiovascular · 86d

Vxtra Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Vxtra Corp.

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