NASAL CANNULA W/2M & 5M TUBING— 510(k) K860872

Name: FDA 510(k) clearance K860872
Creator: U.S. Food and Drug Administration
Published: 1986-03-19

Substantially Equivalent

Dhd Medical Products Div. Diemolding Corp.

FDA 510(k) clearance K860872 for NASAL CANNULA W/2M & 5M TUBING, Substantially Equivalent on 1986-03-19. Applicant: Dhd Medical Products Div. Diemolding Corp.. Device class: 1.

Clearance details

Applicant: Dhd Medical Products Div. Diemolding Corp.
Product code: Code CAT
Device class: Class 1
Regulation: 21 CFR 868.5340
Advisory panel: Anesthesiology
Date received: 1986-02-25
Decision date: 1986-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canastota, NY, US

Download summary PDF View on FDA.gov ↗

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K920573 — CANNULA NASAL OXYGEN1992-08-11

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K881178 — CUFFCHECK1988-04-14
K873498 — INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING1988-03-09
K874047 — ASTHMAKIT1988-02-29

Adverse events under product code CAT

product code CAT

Death: 5
Malfunction: 544
Other: 2
Total: 551

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.