FDA 510(k)

BACTEC 170 TRYPTIC SOY BROTH W/RESINS

K-Number: K830363 · 1983-03-24

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1983-03-24

Product CodeLJF

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

BACTEC 170 TRYPTIC SOY BROTH W/RESINS 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 1983-03-24 under 510(k) number K830363. The device is classified under product code LJF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTEC 170 TRYPTIC SOY BROTH W/RESINS?

BACTEC 170 TRYPTIC SOY BROTH W/RESINS is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K830363.

When did BACTEC 170 TRYPTIC SOY BROTH W/RESINS receive FDA 510(k) clearance?

BACTEC 170 TRYPTIC SOY BROTH W/RESINS received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830363.

Who is the listed applicant for BACTEC 170 TRYPTIC SOY BROTH W/RESINS?

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 BACTEC 170 TRYPTIC SOY BROTH W/RESINS?

The FDA product code for BACTEC 170 TRYPTIC SOY BROTH W/RESINS is LJF.

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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.