MANAN HUBER STYLE INFUSION NEEDLE
K-Number: K883744 · 1988-09-28
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Device Summary
Frequently Asked Questions
What is the MANAN HUBER STYLE INFUSION NEEDLE?
MANAN HUBER STYLE INFUSION NEEDLE is a medical device that received FDA 510(k) clearance on 1988-09-28. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K883744.
When did MANAN HUBER STYLE INFUSION NEEDLE receive FDA 510(k) clearance?
MANAN HUBER STYLE INFUSION NEEDLE received FDA 510(k) clearance on 1988-09-28, under 510(k) number K883744.
Who is the listed applicant for MANAN HUBER STYLE INFUSION NEEDLE?
The FDA 510(k) record lists Manan Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MANAN HUBER STYLE INFUSION NEEDLE?
The FDA product code for MANAN HUBER STYLE INFUSION NEEDLE is FMF.
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 Manan Medical Products, 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.
Related Devices (Code: FMF)
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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