VACUTAINER PLUS TUBES
K-Number: K953463 · 1995-09-20
Advertisement
Device Summary
Frequently Asked Questions
What is the VACUTAINER PLUS TUBES?
VACUTAINER PLUS TUBES is a medical device that received FDA 510(k) clearance on 1995-09-20. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K953463.
When did VACUTAINER PLUS TUBES receive FDA 510(k) clearance?
VACUTAINER PLUS TUBES received FDA 510(k) clearance on 1995-09-20, under 510(k) number K953463.
Who is the listed applicant for VACUTAINER PLUS TUBES?
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 PLUS TUBES?
The FDA product code for VACUTAINER PLUS TUBES 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement