FDA 510(k)

HAEMOPHILUS TEST MEDIUM AGAR (HTM)

K-Number: K962744 · 1996-10-15

ApplicantPrepared Media Laboratory, Inc.

Decision Date1996-10-15

Product CodeJSO

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

HAEMOPHILUS TEST MEDIUM AGAR (HTM) is the device name listed in this FDA 510(k) record. The listed applicant is Prepared Media Laboratory, Inc.. It received FDA 510(k) clearance on 1996-10-15 under 510(k) number K962744. 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 AGAR (HTM)?

HAEMOPHILUS TEST MEDIUM AGAR (HTM) is a medical device that received FDA 510(k) clearance on 1996-10-15. The listed applicant is Prepared Media Laboratory, Inc.. The 510(k) number is K962744.

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

HAEMOPHILUS TEST MEDIUM AGAR (HTM) received FDA 510(k) clearance on 1996-10-15, under 510(k) number K962744.

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

The FDA 510(k) record lists Prepared Media Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAEMOPHILUS TEST MEDIUM AGAR (HTM)?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Prepared Media Laboratory, Inc. as applicant

K962745ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)K782117MARTIN-LEWIS MEDIUM

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.