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FDA 510(k)

HAEMOPHILUS TEST MEDIUM (HTM)AGAR

K-Number: K894216 · 1989-12-13

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1989-12-13
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HAEMOPHILUS TEST MEDIUM (HTM)AGAR 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 1989-12-13 under 510(k) number K894216. 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)AGAR?

HAEMOPHILUS TEST MEDIUM (HTM)AGAR is a medical device that received FDA 510(k) clearance on 1989-12-13. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K894216.

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

HAEMOPHILUS TEST MEDIUM (HTM)AGAR received FDA 510(k) clearance on 1989-12-13, under 510(k) number K894216.

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

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)AGAR?

The FDA product code for HAEMOPHILUS TEST MEDIUM (HTM)AGAR 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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