FDA 510(k)

PISTON SYRINGES

K-Number: K944757 · 1995-01-11

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1995-01-11

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PISTON SYRINGES 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 1995-01-11 under 510(k) number K944757. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PISTON SYRINGES?

PISTON SYRINGES is a medical device that received FDA 510(k) clearance on 1995-01-11. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K944757.

When did PISTON SYRINGES receive FDA 510(k) clearance?

PISTON SYRINGES received FDA 510(k) clearance on 1995-01-11, under 510(k) number K944757.

Who is the listed applicant for PISTON SYRINGES?

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 PISTON SYRINGES?

The FDA product code for PISTON SYRINGES is FMI.

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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.