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FDA 510(k)

LD PRESUMPTO QUAD

K-Number: K871907 · 1987-05-28

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1987-05-28
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LD PRESUMPTO QUAD 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 1987-05-28 under 510(k) number K871907. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LD PRESUMPTO QUAD?

LD PRESUMPTO QUAD is a medical device that received FDA 510(k) clearance on 1987-05-28. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K871907.

When did LD PRESUMPTO QUAD receive FDA 510(k) clearance?

LD PRESUMPTO QUAD received FDA 510(k) clearance on 1987-05-28, under 510(k) number K871907.

Who is the listed applicant for LD PRESUMPTO QUAD?

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 LD PRESUMPTO QUAD?

The FDA product code for LD PRESUMPTO QUAD is JTO.

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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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