CONPHAR NASAL OXYGEN CANNULA-STERILE— 510(k) K791247

Name: FDA 510(k) clearance K791247
Creator: U.S. Food and Drug Administration
Published: 1979-07-24

Substantially Equivalent

Conphar, Inc.

FDA 510(k) clearance K791247 for CONPHAR NASAL OXYGEN CANNULA-STERILE, Substantially Equivalent on 1979-07-24. Applicant: Conphar, Inc.. Device class: 1.

Clearance details

Applicant: Conphar, Inc.
Product code: Code CAT
Device class: Class 1
Regulation: 21 CFR 868.5340
Advisory panel: Anesthesiology
Date received: 1979-07-06
Decision date: 1979-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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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K821295 — OLSEN HEGAR NEEDLE HOLDERS1982-06-03
K821354 — CONPHAR MAYO HEGAR NEEDLE HOLDER1982-06-03
K821248 — ROCHESTER PEAN FORCEPS1982-05-28

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.