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FDA 510(k)

VACUTAINER BRAND BLOOD COLLECTION SYRINGE

K-Number: K982922 · 1998-09-22

Decision Date1998-09-22
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VACUTAINER BRAND BLOOD COLLECTION SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vacutainer Systems. It received FDA 510(k) clearance on 1998-09-22 under 510(k) number K982922. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUTAINER BRAND BLOOD COLLECTION SYRINGE?

VACUTAINER BRAND BLOOD COLLECTION SYRINGE is a medical device that received FDA 510(k) clearance on 1998-09-22. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K982922.

When did VACUTAINER BRAND BLOOD COLLECTION SYRINGE receive FDA 510(k) clearance?

VACUTAINER BRAND BLOOD COLLECTION SYRINGE received FDA 510(k) clearance on 1998-09-22, under 510(k) number K982922.

Who is the listed applicant for VACUTAINER BRAND BLOOD COLLECTION SYRINGE?

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

What is the FDA product code for VACUTAINER BRAND BLOOD COLLECTION SYRINGE?

The FDA product code for VACUTAINER BRAND BLOOD COLLECTION SYRINGE is JKA.

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 Becton Dickinson Vacutainer Systems 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: JKA)

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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