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FDA 510(k)

MICROTECH BACTERIAL CONTROLS

K-Number: K822954 · 1982-11-16

Decision Date1982-11-16
Product CodeJTR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROTECH BACTERIAL CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Universal Micro Reference Laboratory. It received FDA 510(k) clearance on 1982-11-16 under 510(k) number K822954. The device is classified under product code JTR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTECH BACTERIAL CONTROLS?

MICROTECH BACTERIAL CONTROLS is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Universal Micro Reference Laboratory. The 510(k) number is K822954.

When did MICROTECH BACTERIAL CONTROLS receive FDA 510(k) clearance?

MICROTECH BACTERIAL CONTROLS received FDA 510(k) clearance on 1982-11-16, under 510(k) number K822954.

Who is the listed applicant for MICROTECH BACTERIAL CONTROLS?

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

What is the FDA product code for MICROTECH BACTERIAL CONTROLS?

The FDA product code for MICROTECH BACTERIAL CONTROLS is JTR.

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.

Related Devices (Code: JTR)

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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