HUBER NEEDLE INFUSION SET
K-Number: K932638 · 1993-12-14
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Device Summary
Frequently Asked Questions
What is the HUBER NEEDLE INFUSION SET?
HUBER NEEDLE INFUSION SET is a medical device that received FDA 510(k) clearance on 1993-12-14. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K932638.
When did HUBER NEEDLE INFUSION SET receive FDA 510(k) clearance?
HUBER NEEDLE INFUSION SET received FDA 510(k) clearance on 1993-12-14, under 510(k) number K932638.
Who is the listed applicant for HUBER NEEDLE INFUSION SET?
The FDA 510(k) record lists Douglas Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HUBER NEEDLE INFUSION SET?
The FDA product code for HUBER NEEDLE INFUSION SET is FPA.
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 Douglas Medical Products Corp. 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: FPA)
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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