IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER— 510(k) K883592

Unknown

Impra, Inc.

FDA 510(k) clearance K883592 for IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER, Unknown on 1988-12-08. Applicant: Impra, Inc.. Device class: 2.

Clearance details

Applicant: Impra, Inc.
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1988-08-23
Decision date: 1988-12-08
Decision: Unknown
Clearance type: Traditional
Location: Tempe, AZ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LFJ

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K925819 — AKCESS0CATH KIT1994-08-02
K925818 — AKCESS-CATH1994-04-05
K913468 — ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAY1994-03-24
K920634 — SPLITTABLE SHEATH INTRODUCER SET1994-01-14

More clearances from Impra, Inc.

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K991027 — BI-DIRECTIONAL TUNNELER1999-04-22
K983769 — DISTAFLO BYPASS GRAFT1998-12-15
K983861 — DISTAFLO BYPASS GRAFT1998-11-24

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