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)

EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX

K-Number: K870553 · 1987-03-06

Decision Date1987-03-06
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX is the device name listed in this FDA 510(k) record. The listed applicant is Em Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1987-03-06 under 510(k) number K870553. The device is classified under product code JGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX?

EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K870553.

When did EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX receive FDA 510(k) clearance?

EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX received FDA 510(k) clearance on 1987-03-06, under 510(k) number K870553.

Who is the listed applicant for EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX?

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

What is the FDA product code for EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX?

The FDA product code for EASY-TEST MAGNESIUM (MG) ITEM NO. 16XXX is JGJ.

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 Em Diagnostic Systems, 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 288 devices →

Related Devices (Code: JGJ)

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.

↑