QUICVAGE PLUS— 510(k) K914908

Unknown

Autovage

FDA 510(k) clearance K914908 for QUICVAGE PLUS, Unknown on 1992-04-13. Applicant: Autovage. Device class: 2.

Clearance details

Applicant: Autovage
Product code: Code KDH
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1991-11-01
Decision date: 1992-04-13
Decision: Unknown
Clearance type: Traditional
Location: South Park, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KDH

K983624 — GILTECH PLUS CONNECTING TUBE SET1999-03-18
K981286 — SUPERFLOW IRRIGATION AND ASPIRATION TUBING SETS1998-06-19
K971259 — COMBIPORT FLUID LAVAGE DEVICE1997-10-27
K962850 — TUM-E-VAC1997-02-21
K951533 — EASI-LAV PEDIATRIC / ADULT GASTRIC LAVAGE KIT1995-07-05

More clearances from Autovage

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