NO-BOIL SOLID PHASE SIMUL TRAC B12
K-Number: K822721 · 1983-03-10
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Device Summary
Frequently Asked Questions
What is the NO-BOIL SOLID PHASE SIMUL TRAC B12?
NO-BOIL SOLID PHASE SIMUL TRAC B12 is a medical device that received FDA 510(k) clearance on 1983-03-10. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K822721.
When did NO-BOIL SOLID PHASE SIMUL TRAC B12 receive FDA 510(k) clearance?
NO-BOIL SOLID PHASE SIMUL TRAC B12 received FDA 510(k) clearance on 1983-03-10, under 510(k) number K822721.
Who is the listed applicant for NO-BOIL SOLID PHASE SIMUL TRAC B12?
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 NO-BOIL SOLID PHASE SIMUL TRAC B12?
The FDA product code for NO-BOIL SOLID PHASE SIMUL TRAC B12 is CDD.
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.
Related Devices (Code: CDD)
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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