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FDA 510(k)

#19012 CHOCOLATE MUELLER HINTON-150X15MM

K-Number: K820794 · 1982-04-08

Decision Date1982-04-08
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

#19012 CHOCOLATE MUELLER HINTON-150X15MM is the device name listed in this FDA 510(k) record. The listed applicant is Biomedica, Inc.. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820794. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #19012 CHOCOLATE MUELLER HINTON-150X15MM?

#19012 CHOCOLATE MUELLER HINTON-150X15MM is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is Biomedica, Inc.. The 510(k) number is K820794.

When did #19012 CHOCOLATE MUELLER HINTON-150X15MM receive FDA 510(k) clearance?

#19012 CHOCOLATE MUELLER HINTON-150X15MM received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820794.

Who is the listed applicant for #19012 CHOCOLATE MUELLER HINTON-150X15MM?

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

What is the FDA product code for #19012 CHOCOLATE MUELLER HINTON-150X15MM?

The FDA product code for #19012 CHOCOLATE MUELLER HINTON-150X15MM is JTZ.

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.

Other records listing Biomedica, Inc. 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.

View all 19 devices →

Related Devices (Code: JTZ)

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.

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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