ANTIMICROBIAL SUSCEP. TEST, MUELLER
K-Number: K820846 · 1982-04-16
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Device Summary
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.
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
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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