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FDA 510(k)

BECTON DICKINSON MODIFIED MENGHINI NEEDLE

K-Number: K915572 · 1992-02-03

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-02-03
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BECTON DICKINSON MODIFIED MENGHINI NEEDLE 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 1992-02-03 under 510(k) number K915572. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECTON DICKINSON MODIFIED MENGHINI NEEDLE?

BECTON DICKINSON MODIFIED MENGHINI NEEDLE is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K915572.

When did BECTON DICKINSON MODIFIED MENGHINI NEEDLE receive FDA 510(k) clearance?

BECTON DICKINSON MODIFIED MENGHINI NEEDLE received FDA 510(k) clearance on 1992-02-03, under 510(k) number K915572.

Who is the listed applicant for BECTON DICKINSON MODIFIED MENGHINI NEEDLE?

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 BECTON DICKINSON MODIFIED MENGHINI NEEDLE?

The FDA product code for BECTON DICKINSON MODIFIED MENGHINI NEEDLE is GDM.

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Related Devices (Code: GDM)

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.

K071732MARROWMINERStemcor Systems, Inc.K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare CorpK953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.

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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