IV START TRAY— 510(k) K820490

Name: FDA 510(k) clearance K820490
Creator: U.S. Food and Drug Administration
Published: 1982-03-16

Substantially Equivalent

Seamless Hospital Products Co.

FDA 510(k) clearance K820490 for IV START TRAY, Substantially Equivalent on 1982-03-16. Applicant: Seamless Hospital Products Co.. Device class: 2.

Clearance details

Applicant: Seamless Hospital Products Co.
Product code: Code LRS
Device class: Class 2
Regulation: 21 CFR 880.5200
Advisory panel: General Hospital
Date received: 1982-02-23
Decision date: 1982-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Seamless Hospital Products Co.

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K841769 — INTERMITTENT URETHRAL CATHETER TRAY1984-08-24
K823061 — BRUSH, SCRUB, OPERATING ROOM1982-11-05
K821134 — DC PACK TM1982-06-22
K781127 — CONNECTING TUBE, CONDUCTIVE, SURG.1978-09-20

Adverse events under product code LRS

product code LRS

Other: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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