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FDA 510(k)

M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION)

K-Number: K921472 · 1992-05-06

ApplicantMicrotest
Decision Date1992-05-06
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Microtest. It received FDA 510(k) clearance on 1992-05-06 under 510(k) number K921472. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION)?

M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION) is a medical device that received FDA 510(k) clearance on 1992-05-06. The listed applicant is Microtest. The 510(k) number is K921472.

When did M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION) receive FDA 510(k) clearance?

M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION) received FDA 510(k) clearance on 1992-05-06, under 510(k) number K921472.

Who is the listed applicant for M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION)?

The FDA 510(k) record lists Microtest as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION)?

The FDA product code for M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION) is JSM.

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 Microtest as applicant

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.

K941579MODIFIED MICRO TEST MULTI MICROBE MEDIUM (M5)K914894VIRAPURE, CHLAMYPURE AND MYCOPUREK910526MICROTEST MULTI MICROBE MEDIUM

Related Devices (Code: JSM)

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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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.

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