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FDA 510(k)

CONPHAR OXYGEN CATHETER-STERILE

K-Number: K791273 · 1979-07-24

ApplicantConphar, Inc.
Decision Date1979-07-24
Product CodeBZB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONPHAR OXYGEN CATHETER-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-07-24 under 510(k) number K791273. The device is classified under product code BZB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR OXYGEN CATHETER-STERILE?

CONPHAR OXYGEN CATHETER-STERILE is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Conphar, Inc.. The 510(k) number is K791273.

When did CONPHAR OXYGEN CATHETER-STERILE receive FDA 510(k) clearance?

CONPHAR OXYGEN CATHETER-STERILE received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791273.

Who is the listed applicant for CONPHAR OXYGEN CATHETER-STERILE?

The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONPHAR OXYGEN CATHETER-STERILE?

The FDA product code for CONPHAR OXYGEN CATHETER-STERILE is BZB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Conphar, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 122 devices →

Related Devices (Code: BZB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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