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FDA 510(k)

VACUTAINER BRAND PPT PLASMA PREPARATION TUBE

K-Number: K972075 · 1998-02-24

Decision Date1998-02-24
Product CodePJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VACUTAINER BRAND PPT PLASMA PREPARATION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vacutainer Systems. It received FDA 510(k) clearance on 1998-02-24 under 510(k) number K972075. The device is classified under product code PJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUTAINER BRAND PPT PLASMA PREPARATION TUBE?

VACUTAINER BRAND PPT PLASMA PREPARATION TUBE is a medical device that received FDA 510(k) clearance on 1998-02-24. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K972075.

When did VACUTAINER BRAND PPT PLASMA PREPARATION TUBE receive FDA 510(k) clearance?

VACUTAINER BRAND PPT PLASMA PREPARATION TUBE received FDA 510(k) clearance on 1998-02-24, under 510(k) number K972075.

Who is the listed applicant for VACUTAINER BRAND PPT PLASMA PREPARATION TUBE?

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 PPT PLASMA PREPARATION TUBE?

The FDA product code for VACUTAINER BRAND PPT PLASMA PREPARATION TUBE is PJE.

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.

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Related Devices (Code: PJE)

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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