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FDA 510(k)

BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI.

K-Number: K882556 · 1988-09-15

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-09-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI. 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 1988-09-15 under 510(k) number K882556. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI.?

BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI. is a medical device that received FDA 510(k) clearance on 1988-09-15. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K882556.

When did BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI. receive FDA 510(k) clearance?

BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI. received FDA 510(k) clearance on 1988-09-15, under 510(k) number K882556.

Who is the listed applicant for BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI.?

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 BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI.?

The FDA product code for BECTON DICKINSON PCA INFUSER - SOFTWARE MODIFI. is FRN.

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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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