Medical Device Manufacturer · US , Minneapolis , MN

Schneider-Shilley (Usa) - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1988

Total

Cleared

Denied

Schneider-Shilley (Usa) has 9 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 9 cleared submissions from 1988 to 1989. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Schneider-Shilley (Usa) Filter by specialty or product code using the sidebar.

Schneider-Shilley (Usa) 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 - Schneider-Shilley (Usa)

9 devices

1-9 of 9

Cleared Jan 24, 1989

SOFTRAC-PTA PERIPHERAL DILATATION CATHETER

K882826 · LIT

Cardiovascular · 200d

Cleared Jul 28, 1988

MODIFIED PERIPHERAL DILATATION CATHETERS

K875175 · LIT

Cardiovascular · 224d

Cleared May 16, 1988

SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETER

K881197 · LIT

Cardiovascular · 56d

Cleared Mar 28, 1988

MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER

K875322 · KRK

Cardiovascular · 90d

Cleared Mar 28, 1988

MODIFIED SCHNEIDER-SHILEY WIRE TORQUER

K875323 · DQX

Cardiovascular · 90d

Cleared Mar 25, 1988

MODIFIED SCHNEIDER SHILEY INFLATION SYRINGES

K875324 · DXT

Cardiovascular · 87d

Cleared Mar 25, 1988

MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENT

K875327 · DRE

Cardiovascular · 87d

Cleared Feb 18, 1988

MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK

K875325 · DQO

Cardiovascular · 51d

Cleared Feb 18, 1988

MODIFIED SCHNEIDER-SHILEY FLUSHING CATHETER

K875326 · DQO

Cardiovascular · 51d

Schneider-Shilley (Usa) - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Schneider-Shilley (Usa)

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