MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER— 510(k) K875322

Name: FDA 510(k) clearance K875322
Creator: U.S. Food and Drug Administration
Published: 1988-03-28

Substantially Equivalent

Schneider-Shilley (Usa)

FDA 510(k) clearance K875322 for MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER, Substantially Equivalent on 1988-03-28. Applicant: Schneider-Shilley (Usa). Device class: 2.

Clearance details

Applicant: Schneider-Shilley (Usa)
Product code: Code KRK
Device class: Class 2
Regulation: 21 CFR 870.1140
Advisory panel: Cardiovascular
Date received: 1987-12-29
Decision date: 1988-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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Recent devices under product code KRK

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K950607 — UST-5268P-5 TRANSDUCER1995-09-15
K904674 — CENTRAL VENOUS PRESSURE MANOMETER1990-12-27
K884386 — ADMINISTRATION/MANOMETER SET W/3 WAY STOPCOCK1989-01-05
K861605 — SCHNEIDER-SHILEY PRESSURE MANOMETER1986-05-28
K830910 — MANOMETER SET C.V.P. #S 298/2991983-04-05

More clearances from Schneider-Shilley (Usa)

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K882826 — SOFTRAC-PTA PERIPHERAL DILATATION CATHETER1989-01-24
K875175 — MODIFIED PERIPHERAL DILATATION CATHETERS1988-07-28
K881197 — SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETER1988-05-16
K875323 — MODIFIED SCHNEIDER-SHILEY WIRE TORQUER1988-03-28
K875324 — MODIFIED SCHNEIDER SHILEY INFLATION SYRINGES1988-03-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.