VENESECTION EQUIPMENT STORAGE TRAY— 510(k) K862154

Name: FDA 510(k) clearance K862154
Creator: U.S. Food and Drug Administration
Published: 1986-06-16

Substantially Equivalent

Rmp Co.

FDA 510(k) clearance K862154 for VENESECTION EQUIPMENT STORAGE TRAY, Substantially Equivalent on 1986-06-16. Applicant: Rmp Co.. Device class: 1.

Clearance details

Applicant: Rmp Co.
Product code: Code FSM
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1986-06-05
Decision date: 1986-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fayetteville, NC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FSM

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K971217 — INSTRUMENT TRAY LINER1997-05-06
K962328 — SINGLE USE INSTRUMENT TRAY1996-08-09
K944025 — SURGICAL INSTRUMENT TRAY1994-11-22
K912106 — ARTHROSCOPY TRAY1991-08-29
K912053 — OPEN HEART TRAY1991-08-26

More clearances from Rmp Co.

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K862197 — RMP COMPANT CRICOTHYROTOMY EQUIPMENT STORAGE TRAY1986-06-19
K832697 — RMP INTUBATION EQUIP. STORAGE TRAY1983-12-27

Adverse events under product code FSM

product code FSM

Malfunction: 1,289
Total: 1,289

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.