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FDA 510(k)

ANTIMICROBIAL SUSCEP. TEST, MUELLER

K-Number: K820846 · 1982-04-16

Decision Date1982-04-16
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL SUSCEP. TEST, MUELLER is the device name listed in this FDA 510(k) record. The listed applicant is Blue Ridge Media Co.. It received FDA 510(k) clearance on 1982-04-16 under 510(k) number K820846. 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 ANTIMICROBIAL SUSCEP. TEST, MUELLER?

ANTIMICROBIAL SUSCEP. TEST, MUELLER is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Blue Ridge Media Co.. The 510(k) number is K820846.

When did ANTIMICROBIAL SUSCEP. TEST, MUELLER receive FDA 510(k) clearance?

ANTIMICROBIAL SUSCEP. TEST, MUELLER received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820846.

Who is the listed applicant for ANTIMICROBIAL SUSCEP. TEST, MUELLER?

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

What is the FDA product code for ANTIMICROBIAL SUSCEP. TEST, MUELLER?

The FDA product code for ANTIMICROBIAL SUSCEP. TEST, MUELLER 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 Blue Ridge Media Co. 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 11 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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