Conphar Oxygen Catheter-Sterile

FDA 510(k) K791273 · Conphar, Inc.

Substantially Equivalent

510(k) numberK791273

Submission

Device name
Conphar Oxygen Catheter-Sterile
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
July 6, 1979
Decision date
July 24, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BZB – Catheter, Nasal, Oxygen
Device class
Class I (low risk)
Regulation
21 CFR 868.5350
Specialty
Anesthesiology

Other 510(k)s with product code BZB

510(k)DeviceApplicantDecision
K896731Oxygen CathetersBZB · Traditional Unoplast A/S03/30/1990SE
K843466Pharma-Plast Oxygen CatheterBZB · Traditional Zimmar Consulting , Ltd.11/19/1984SE
K833351Demand Oxygen ControllerBZB · Traditional Healthdyne, Inc.03/19/1984SE
K830984Oxygen CathetersBZB · Traditional Medovations, Inc.05/18/1983SE
K820370Nasal Oxygen CatheterBZB · Traditional American Pharmaseal Div. Ahsc04/16/1982SE
K800506Oxygen CatheterBZB · Traditional Medi-Craft , Ltd.03/25/1980SE
K790057Catheter, OxygenBZB · Traditional Medline Industries, Inc.02/05/1979SE

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Questions and answers

When was Conphar Oxygen Catheter-Sterile cleared by the FDA?

Conphar Oxygen Catheter-Sterile (K791273) received a 510(k) decision of Substantially Equivalent on July 24, 1979, 18 days after the submission was received.

What is the product code of K791273?

The FDA product code is BZB – Catheter, Nasal, Oxygen, a Class I (low risk) device regulated under 21 CFR 868.5350.