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FDA 510(k)

HAEMOPHILUS TEST MEDIUM (HTM) BROTH

K-Number: K903425 · 1990-08-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1990-08-22
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HAEMOPHILUS TEST MEDIUM (HTM) BROTH 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 1990-08-22 under 510(k) number K903425. The device is classified under product code JSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAEMOPHILUS TEST MEDIUM (HTM) BROTH?

HAEMOPHILUS TEST MEDIUM (HTM) BROTH is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K903425.

When did HAEMOPHILUS TEST MEDIUM (HTM) BROTH receive FDA 510(k) clearance?

HAEMOPHILUS TEST MEDIUM (HTM) BROTH received FDA 510(k) clearance on 1990-08-22, under 510(k) number K903425.

Who is the listed applicant for HAEMOPHILUS TEST MEDIUM (HTM) BROTH?

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 HAEMOPHILUS TEST MEDIUM (HTM) BROTH?

The FDA product code for HAEMOPHILUS TEST MEDIUM (HTM) BROTH is JSO.

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Related Devices (Code: JSO)

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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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