EXEL HUBER INFUSION SET ROTATING WING
K-Number: K926119 · 1993-08-11
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Device Summary
Frequently Asked Questions
What is the EXEL HUBER INFUSION SET ROTATING WING?
EXEL HUBER INFUSION SET ROTATING WING is a medical device that received FDA 510(k) clearance on 1993-08-11. The listed applicant is Exel Intl.. The 510(k) number is K926119.
When did EXEL HUBER INFUSION SET ROTATING WING receive FDA 510(k) clearance?
EXEL HUBER INFUSION SET ROTATING WING received FDA 510(k) clearance on 1993-08-11, under 510(k) number K926119.
Who is the listed applicant for EXEL HUBER INFUSION SET ROTATING WING?
The FDA 510(k) record lists Exel Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXEL HUBER INFUSION SET ROTATING WING?
The FDA product code for EXEL HUBER INFUSION SET ROTATING WING 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 Exel Intl. 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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