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FDA 510(k)

ANTIMICROBIAL SUSCEPT-CULTURE MEDIA

K-Number: K841213 · 1984-04-04

Decision Date1984-04-04
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL SUSCEPT-CULTURE MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Smith River Biologicals. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K841213. 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 SUSCEPT-CULTURE MEDIA?

ANTIMICROBIAL SUSCEPT-CULTURE MEDIA is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Smith River Biologicals. The 510(k) number is K841213.

When did ANTIMICROBIAL SUSCEPT-CULTURE MEDIA receive FDA 510(k) clearance?

ANTIMICROBIAL SUSCEPT-CULTURE MEDIA received FDA 510(k) clearance on 1984-04-04, under 510(k) number K841213.

Who is the listed applicant for ANTIMICROBIAL SUSCEPT-CULTURE MEDIA?

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

What is the FDA product code for ANTIMICROBIAL SUSCEPT-CULTURE MEDIA?

The FDA product code for ANTIMICROBIAL SUSCEPT-CULTURE MEDIA 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 Smith River Biologicals 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 12 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

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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