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FDA 510(k)

AUTO ISO-FILTER COLLECTION TUBE CAP

K-Number: K780303 · 1978-03-30

Decision Date1978-03-30
Product CodeGJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTO ISO-FILTER COLLECTION TUBE CAP is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1978-03-30 under 510(k) number K780303. The device is classified under product code GJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 632 devices →

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

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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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