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FDA 510(k)

B-D SAFETY-LOK(TM) I.V. NEEDLES

K-Number: K911136 · 1991-06-14

Decision Date1991-06-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

B-D SAFETY-LOK(TM) I.V. NEEDLES 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 1991-06-14 under 510(k) number K911136. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 632 devices →

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

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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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