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FDA 510(k)

BECTON DICKINSON SYRINGE

K-Number: K980987 · 1998-06-11

Decision Date1998-06-11
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BECTON DICKINSON SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1998-06-11 under 510(k) number K980987. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECTON DICKINSON SYRINGE?

BECTON DICKINSON SYRINGE is a medical device that received FDA 510(k) clearance on 1998-06-11. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K980987.

When did BECTON DICKINSON SYRINGE receive FDA 510(k) clearance?

BECTON DICKINSON SYRINGE received FDA 510(k) clearance on 1998-06-11, under 510(k) number K980987.

Who is the listed applicant for BECTON DICKINSON SYRINGE?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BECTON DICKINSON SYRINGE?

The FDA product code for BECTON DICKINSON SYRINGE is FMF.

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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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.

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Related Devices (Code: FMF)

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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