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)

EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420

K-Number: K893915 · 1989-08-31

Decision Date1989-08-31
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420 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 1989-08-31 under 510(k) number K893915. The device is classified under product code CEK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420?

EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420 is a medical device that received FDA 510(k) clearance on 1989-08-31. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K893915.

When did EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420 receive FDA 510(k) clearance?

EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420 received FDA 510(k) clearance on 1989-08-31, under 510(k) number K893915.

Who is the listed applicant for EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420?

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 EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420?

The FDA product code for EMDS TOTAL PROTEIN (TP), ITEM NUMBER 65420 is CEK.

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: CEK)

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.

↑