CANNULA, DISPOSABLE OXYGEN TTHERAPY— 510(k) K760330

Name: FDA 510(k) clearance K760330
Creator: U.S. Food and Drug Administration
Published: 1976-08-04

Substantially Equivalent

Inhal-O-Tech Medical Plastic

FDA 510(k) clearance K760330 for CANNULA, DISPOSABLE OXYGEN TTHERAPY, Substantially Equivalent on 1976-08-04. Applicant: Inhal-O-Tech Medical Plastic. Device class: 1.

Clearance details

Applicant: Inhal-O-Tech Medical Plastic
Product code: Code CAT
Device class: Class 1
Regulation: 21 CFR 868.5340
Advisory panel: Anesthesiology
Date received: 1976-07-28
Decision date: 1976-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Blue Springs, MO, US

Download summary PDF View on FDA.gov ↗

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K921496 — SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED1992-08-14
K920573 — CANNULA NASAL OXYGEN1992-08-11

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K781741 — MASK, BI FLO NASAL OXYGEN1978-12-01
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K781395 — DISPOSABLE AEROSOL T BRIGGS ADAPTOR1978-08-31
K770353 — DISPOSABLE TEMPERATURE PROBE1977-03-16
K770354 — TUBING, AEROSAL, DISPOSABLE1977-03-16

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.