VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.— 510(k) K922997

Name: FDA 510(k) clearance K922997
Creator: U.S. Food and Drug Administration
Published: 1994-01-11

Unknown

Via Medical Corp.

FDA 510(k) clearance K922997 for VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD., Unknown on 1994-01-11. Applicant: Via Medical Corp.. Device class: 2.

Clearance details

Applicant: Via Medical Corp.
Product code: Code LZF
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1992-06-22
Decision date: 1994-01-11
Decision: Unknown
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K922997

K-number listed on FDA's recall record

Z-1531-2013 — VIA Medical Collection Bag; The collection bag is an accessory waste bag used in conjunction with the sterile LVM blood gas sensor with the LVM Monitor. The collection bag is packaged in a tyvek pouch which is included in either replacement kit (777-3103) or LVM sensor kit (777-3102).Class II·Terminated·International Biomedical, Ltd.·20130524

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K922997.

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