FDA 510(k)

BECTEC NR-660 BACTERIAL DETECT SYS

K-Number: K842279 · 1984-07-20

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1984-07-20

Product CodeJTA

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

BECTEC NR-660 BACTERIAL DETECT SYS 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 1984-07-20 under 510(k) number K842279. The device is classified under product code JTA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECTEC NR-660 BACTERIAL DETECT SYS?

BECTEC NR-660 BACTERIAL DETECT SYS is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K842279.

When did BECTEC NR-660 BACTERIAL DETECT SYS receive FDA 510(k) clearance?

BECTEC NR-660 BACTERIAL DETECT SYS received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842279.

Who is the listed applicant for BECTEC NR-660 BACTERIAL DETECT SYS?

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 BECTEC NR-660 BACTERIAL DETECT SYS?

The FDA product code for BECTEC NR-660 BACTERIAL DETECT SYS is JTA.

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Related Devices (Code: JTA)

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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.