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FDA 510(k)

STERILE NEEDLE FOR BLOOD COLLECTION

K-Number: K880746 · 1988-05-31

Decision Date1988-05-31
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE NEEDLE FOR BLOOD COLLECTION is the device name listed in this FDA 510(k) record. The listed applicant is Applied Plastics Technology, Inc.. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K880746. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE NEEDLE FOR BLOOD COLLECTION?

STERILE NEEDLE FOR BLOOD COLLECTION is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Applied Plastics Technology, Inc.. The 510(k) number is K880746.

When did STERILE NEEDLE FOR BLOOD COLLECTION receive FDA 510(k) clearance?

STERILE NEEDLE FOR BLOOD COLLECTION received FDA 510(k) clearance on 1988-05-31, under 510(k) number K880746.

Who is the listed applicant for STERILE NEEDLE FOR BLOOD COLLECTION?

The FDA 510(k) record lists Applied Plastics Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE NEEDLE FOR BLOOD COLLECTION?

The FDA product code for STERILE NEEDLE FOR BLOOD COLLECTION 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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