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FDA 510(k)

BEAVER(R) HANDLE

K-Number: K884512 · 1988-11-17

Decision Date1988-11-17
Product CodeGDZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BEAVER(R) HANDLE 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 1988-11-17 under 510(k) number K884512. The device is classified under product code GDZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAVER(R) HANDLE?

BEAVER(R) HANDLE is a medical device that received FDA 510(k) clearance on 1988-11-17. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K884512.

When did BEAVER(R) HANDLE receive FDA 510(k) clearance?

BEAVER(R) HANDLE received FDA 510(k) clearance on 1988-11-17, under 510(k) number K884512.

Who is the listed applicant for BEAVER(R) HANDLE?

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 BEAVER(R) HANDLE?

The FDA product code for BEAVER(R) HANDLE is GDZ.

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: GDZ)

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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