Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CULTURIA MACCONKEY-MUG

K-Number: K934759 · 1994-09-09

Decision Date1994-09-09
Product CodeJXA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURIA MACCONKEY-MUG is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Convenience Products, Inc.. It received FDA 510(k) clearance on 1994-09-09 under 510(k) number K934759. The device is classified under product code JXA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CULTURIA MACCONKEY-MUG?

CULTURIA MACCONKEY-MUG is a medical device that received FDA 510(k) clearance on 1994-09-09. The listed applicant is Clinical Convenience Products, Inc.. The 510(k) number is K934759.

When did CULTURIA MACCONKEY-MUG receive FDA 510(k) clearance?

CULTURIA MACCONKEY-MUG received FDA 510(k) clearance on 1994-09-09, under 510(k) number K934759.

Who is the listed applicant for CULTURIA MACCONKEY-MUG?

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

What is the FDA product code for CULTURIA MACCONKEY-MUG?

The FDA product code for CULTURIA MACCONKEY-MUG is JXA.

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 Clinical Convenience Products, 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.

Related Devices (Code: JXA)

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.

↑