HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER
K-Number: K883133 · 1988-11-21
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Device Summary
Frequently Asked Questions
What is the HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER?
HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER is a medical device that received FDA 510(k) clearance on 1988-11-21. The listed applicant is Ferguson Medical. The 510(k) number is K883133.
When did HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER receive FDA 510(k) clearance?
HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER received FDA 510(k) clearance on 1988-11-21, under 510(k) number K883133.
Who is the listed applicant for HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER?
The FDA 510(k) record lists Ferguson Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER?
The FDA product code for HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER is FOX.
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 Ferguson Medical 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: FOX)
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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