PHARMA-PLAST OXYGEN CATHETER
K-Number: K843466 · 1984-11-19
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Device Summary
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.
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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