AUTO ISO-FILTER COLLECTION TUBE CAP
K-Number: K780303 · 1978-03-30
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Device Summary
Frequently Asked Questions
What is the AUTO ISO-FILTER COLLECTION TUBE CAP?
AUTO ISO-FILTER COLLECTION TUBE CAP is a medical device that received FDA 510(k) clearance on 1978-03-30. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K780303.
When did AUTO ISO-FILTER COLLECTION TUBE CAP receive FDA 510(k) clearance?
AUTO ISO-FILTER COLLECTION TUBE CAP received FDA 510(k) clearance on 1978-03-30, under 510(k) number K780303.
Who is the listed applicant for AUTO ISO-FILTER COLLECTION TUBE CAP?
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 AUTO ISO-FILTER COLLECTION TUBE CAP?
The FDA product code for AUTO ISO-FILTER COLLECTION TUBE CAP is GJE.
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: GJE)
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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