BLOOD COLLECTING NEEDLE AND HOLDERS
K-Number: K880892 · 1988-04-21
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Device Summary
Frequently Asked Questions
What is the BLOOD COLLECTING NEEDLE AND HOLDERS?
BLOOD COLLECTING NEEDLE AND HOLDERS is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K880892.
When did BLOOD COLLECTING NEEDLE AND HOLDERS receive FDA 510(k) clearance?
BLOOD COLLECTING NEEDLE AND HOLDERS received FDA 510(k) clearance on 1988-04-21, under 510(k) number K880892.
Who is the listed applicant for BLOOD COLLECTING NEEDLE AND HOLDERS?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD COLLECTING NEEDLE AND HOLDERS?
The FDA product code for BLOOD COLLECTING NEEDLE AND HOLDERS is FMI.
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 Abco Dealers, 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: FMI)
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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