PHARMA-PLAST CONNECTING TUBE TYPE URIN-
K-Number: K843481 · 1984-10-18
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Device Summary
Frequently Asked Questions
What is the PHARMA-PLAST CONNECTING TUBE TYPE URIN-?
PHARMA-PLAST CONNECTING TUBE TYPE URIN- is a medical device that received FDA 510(k) clearance on 1984-10-18. The listed applicant is Zimmar Consulting , Ltd.. The 510(k) number is K843481.
When did PHARMA-PLAST CONNECTING TUBE TYPE URIN- receive FDA 510(k) clearance?
PHARMA-PLAST CONNECTING TUBE TYPE URIN- received FDA 510(k) clearance on 1984-10-18, under 510(k) number K843481.
Who is the listed applicant for PHARMA-PLAST CONNECTING TUBE TYPE URIN-?
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 CONNECTING TUBE TYPE URIN-?
The FDA product code for PHARMA-PLAST CONNECTING TUBE TYPE URIN- is KNX.
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: KNX)
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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