ANESTHESIA TRAY, CAUDAL— 510(k) K780120

Name: FDA 510(k) clearance K780120
Creator: U.S. Food and Drug Administration
Published: 1978-02-06

Substantially Equivalent

Kendall Research Center

FDA 510(k) clearance K780120 for ANESTHESIA TRAY, CAUDAL, Substantially Equivalent on 1978-02-06. Applicant: Kendall Research Center. Device class: 2.

Clearance details

Applicant: Kendall Research Center
Product code: Code CAZ
Device class: Class 2
Regulation: 21 CFR 868.5140
Advisory panel: Anesthesiology
Date received: 1978-01-23
Decision date: 1978-02-06
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 Kendall Research Center

view all

K802225 — TENDER-SORB DRAIN SPONGES1980-09-26
K781357 — T.E.D. SEQUENTIAL COMPRESSION SLEEVES1978-09-20
K780408 — MICRONET LIGHT DRESSING SPONGE1978-03-22
K780062 — CATHETER/HEMOSTATIC/GERIATRIC1978-02-14
K772133 — URINE SPECIMEN COLLECTING DEVICE1977-11-28

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.