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FDA 510(k)

MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992

K-Number: K002456 · 2000-11-02

Decision Date2000-11-02
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 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 2000-11-02 under 510(k) number K002456. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992?

MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 is a medical device that received FDA 510(k) clearance on 2000-11-02. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K002456.

When did MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 receive FDA 510(k) clearance?

MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 received FDA 510(k) clearance on 2000-11-02, under 510(k) number K002456.

Who is the listed applicant for MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992?

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 MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992?

The FDA product code for MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 is JKA.

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.

View all 15 devices →

Related Devices (Code: JKA)

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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