LOK-ON NEEDLE DISPOSAL SYSTEM
K-Number: K951886 · 1995-06-30
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Device Summary
Frequently Asked Questions
What is the LOK-ON NEEDLE DISPOSAL SYSTEM?
LOK-ON NEEDLE DISPOSAL SYSTEM is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Becton Dickinson Vacutainer Systems. The 510(k) number is K951886.
When did LOK-ON NEEDLE DISPOSAL SYSTEM receive FDA 510(k) clearance?
LOK-ON NEEDLE DISPOSAL SYSTEM received FDA 510(k) clearance on 1995-06-30, under 510(k) number K951886.
Who is the listed applicant for LOK-ON NEEDLE DISPOSAL SYSTEM?
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 LOK-ON NEEDLE DISPOSAL SYSTEM?
The FDA product code for LOK-ON NEEDLE DISPOSAL SYSTEM is GIM.
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.
Related Devices (Code: GIM)
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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