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)

THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR

K-Number: K844526 · 1985-01-07

Decision Date1985-01-07
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1985-01-07 under 510(k) number K844526. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR?

THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR is a medical device that received FDA 510(k) clearance on 1985-01-07. The listed applicant is bioMerieux, Inc.. The 510(k) number is K844526.

When did THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR receive FDA 510(k) clearance?

THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844526.

Who is the listed applicant for THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR?

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

What is the FDA product code for THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR?

The FDA product code for THIOGLYCOLLATE W/O DEXTROSE OR INDICATOR is JSG.

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 bioMerieux, 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.

View all 248 devices →

Related Devices (Code: JSG)

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.

↑