FUNNEL ADAPTOR
K-Number: K923265 · 1993-03-18
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Device Summary
Frequently Asked Questions
What is the FUNNEL ADAPTOR?
FUNNEL ADAPTOR is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Southmedic, Inc.. The 510(k) number is K923265.
When did FUNNEL ADAPTOR receive FDA 510(k) clearance?
FUNNEL ADAPTOR received FDA 510(k) clearance on 1993-03-18, under 510(k) number K923265.
Who is the listed applicant for FUNNEL ADAPTOR?
The FDA 510(k) record lists Southmedic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FUNNEL ADAPTOR?
The FDA product code for FUNNEL ADAPTOR is CAD.
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 Southmedic, 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: CAD)
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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