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FDA 510(k)

BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU

K-Number: K854986 · 1986-01-03

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1986-01-03
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU 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 1986-01-03 under 510(k) number K854986. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU?

BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU is a medical device that received FDA 510(k) clearance on 1986-01-03. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K854986.

When did BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU receive FDA 510(k) clearance?

BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU received FDA 510(k) clearance on 1986-01-03, under 510(k) number K854986.

Who is the listed applicant for BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU?

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 BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU?

The FDA product code for BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU is JSM.

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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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