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FDA 510(k)

PHARMA-PLAST OXYGEN CATHETER

K-Number: K843466 · 1984-11-19

Decision Date1984-11-19
Product CodeBZB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PHARMA-PLAST OXYGEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Zimmar Consulting , Ltd.. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K843466. 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 PHARMA-PLAST OXYGEN CATHETER?

PHARMA-PLAST OXYGEN CATHETER is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Zimmar Consulting , Ltd.. The 510(k) number is K843466.

When did PHARMA-PLAST OXYGEN CATHETER receive FDA 510(k) clearance?

PHARMA-PLAST OXYGEN CATHETER received FDA 510(k) clearance on 1984-11-19, under 510(k) number K843466.

Who is the listed applicant for PHARMA-PLAST OXYGEN CATHETER?

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

What is the FDA product code for PHARMA-PLAST OXYGEN CATHETER?

The FDA product code for PHARMA-PLAST OXYGEN CATHETER 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 Zimmar Consulting , Ltd. 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 17 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

View on FDA Database →

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

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