TRAY, STERILE DISPOSABLE ARTHROGRAM— 510(k) K760249

Name: FDA 510(k) clearance K760249
Creator: U.S. Food and Drug Administration
Published: 1976-08-04

Substantially Equivalent

Travenol Laboratories, S.A.

FDA 510(k) clearance K760249 for TRAY, STERILE DISPOSABLE ARTHROGRAM, Substantially Equivalent on 1976-08-04. Applicant: Travenol Laboratories, S.A.. Device class: 2.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code CAZ
Device class: Class 2
Regulation: 21 CFR 868.5140
Advisory panel: Anesthesiology
Date received: 1976-07-19
Decision date: 1976-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAZ

view all

K222341 — Arrow 0.2 Micron Flat Filter, GVS2023-02-13
K210983 — BD Epilor Syringe2022-05-19
K201356 — Plastic LOR Syringe2021-02-12
K202699 — E-Cath STIM acc. Tsui2020-12-29
K190345 — VPC2019-05-16

More clearances from Travenol Laboratories, S.A.

view all

K874181 — BAXTER BEDSIDE SYSTEM1988-02-22
K873894 — CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE1987-11-05
K873873 — RESUBMITTED MICRON TRANSFUSION FILTER1987-10-22
K873984 — AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)1987-10-20
K872364 — HEMODIALYSIS (SPS), MODEL 550, CODE 5M13091987-10-13

Adverse events under product code CAZ

product code CAZ

Injury: 145
Malfunction: 942
Other: 1
Total: 1,088

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.