# Schneider-Shilley (Usa)

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 9 (1988–1989): 9 510(k) clearances
- Product codes: LIT (3), DQO (2), DXT (1), KRK (1), DQX (1), DRE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K882826: Softrac-Pta Peripheral Dilatation Catheter (Jan 24, 1989)
- K875175: Modified Peripheral Dilatation Catheters (Jul 28, 1988)
- K881197: Softrac-Pta (TM) Peripheral Dilatation Catheter (May 16, 1988)
- K875322: Modified Schneider-Shiley Pressure Manometer (Mar 28, 1988)
- K875323: Modified Schneider-Shiley Wire Torquer (Mar 28, 1988)
- K875324: Modified Schneider Shiley Inflation Syringes (Mar 25, 1988)
- K875327: Modified Seldinger Initial Puncture Instrument (Mar 25, 1988)
- K875326: Modified Schneider-Shiley Flushing Catheter (Feb 18, 1988)

Source page: https://510kreport.com/company/schneider-shilley-usa