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FDA 510(k)

B-D ULTRA FINE(R) LANCET

K-Number: K932725 · 1993-07-23

Decision Date1993-07-23
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

B-D ULTRA FINE(R) LANCET 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 1993-07-23 under 510(k) number K932725. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B-D ULTRA FINE(R) LANCET?

B-D ULTRA FINE(R) LANCET is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K932725.

When did B-D ULTRA FINE(R) LANCET receive FDA 510(k) clearance?

B-D ULTRA FINE(R) LANCET received FDA 510(k) clearance on 1993-07-23, under 510(k) number K932725.

Who is the listed applicant for B-D ULTRA FINE(R) LANCET?

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 ULTRA FINE(R) LANCET?

The FDA product code for B-D ULTRA FINE(R) LANCET is FMK.

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: FMK)

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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