B-D SAFETY-LOK(TM) I.V. NEEDLES
K-Number: K911136 · 1991-06-14
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Device Summary
Frequently Asked Questions
What is the B-D SAFETY-LOK(TM) I.V. NEEDLES?
B-D SAFETY-LOK(TM) I.V. NEEDLES is a medical device that received FDA 510(k) clearance on 1991-06-14. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K911136.
When did B-D SAFETY-LOK(TM) I.V. NEEDLES receive FDA 510(k) clearance?
B-D SAFETY-LOK(TM) I.V. NEEDLES received FDA 510(k) clearance on 1991-06-14, under 510(k) number K911136.
Who is the listed applicant for B-D SAFETY-LOK(TM) I.V. NEEDLES?
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 B-D SAFETY-LOK(TM) I.V. NEEDLES?
The FDA product code for B-D SAFETY-LOK(TM) I.V. NEEDLES is FPA.
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.
Related Devices (Code: FPA)
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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