VACUTAINER BRAND PLUS SERUM & SST TUBES
K-Number: K960250 · 1996-03-29
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Device Summary
Frequently Asked Questions
What is the VACUTAINER BRAND PLUS SERUM & SST TUBES?
VACUTAINER BRAND PLUS SERUM & SST TUBES is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K960250.
When did VACUTAINER BRAND PLUS SERUM & SST TUBES receive FDA 510(k) clearance?
VACUTAINER BRAND PLUS SERUM & SST TUBES received FDA 510(k) clearance on 1996-03-29, under 510(k) number K960250.
Who is the listed applicant for VACUTAINER BRAND PLUS SERUM & SST 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 BRAND PLUS SERUM & SST TUBES?
The FDA product code for VACUTAINER BRAND PLUS SERUM & SST 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.
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