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FDA 510(k)

VACUTAINER BRAND CTAD TUBE (MULTIPLE)

K-Number: K991120 · 1999-05-19

Decision Date1999-05-19
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VACUTAINER BRAND CTAD TUBE (MULTIPLE) 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 1999-05-19 under 510(k) number K991120. 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 CTAD TUBE (MULTIPLE)?

VACUTAINER BRAND CTAD TUBE (MULTIPLE) is a medical device that received FDA 510(k) clearance on 1999-05-19. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K991120.

When did VACUTAINER BRAND CTAD TUBE (MULTIPLE) receive FDA 510(k) clearance?

VACUTAINER BRAND CTAD TUBE (MULTIPLE) received FDA 510(k) clearance on 1999-05-19, under 510(k) number K991120.

Who is the listed applicant for VACUTAINER BRAND CTAD TUBE (MULTIPLE)?

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 CTAD TUBE (MULTIPLE)?

The FDA product code for VACUTAINER BRAND CTAD TUBE (MULTIPLE) 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.

View all 15 devices →

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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