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FDA 510(k)

ES600 IMMUNOASSAY SYSTEM

K-Number: K860647 · 1986-04-17

Decision Date1986-04-17
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ES600 IMMUNOASSAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1986-04-17 under 510(k) number K860647. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ES600 IMMUNOASSAY SYSTEM?

ES600 IMMUNOASSAY SYSTEM is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K860647.

When did ES600 IMMUNOASSAY SYSTEM receive FDA 510(k) clearance?

ES600 IMMUNOASSAY SYSTEM received FDA 510(k) clearance on 1986-04-17, under 510(k) number K860647.

Who is the listed applicant for ES600 IMMUNOASSAY SYSTEM?

The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ES600 IMMUNOASSAY SYSTEM?

The FDA product code for ES600 IMMUNOASSAY SYSTEM is JJE.

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 Boehringer Mannheim Corp. 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.

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Related Devices (Code: JJE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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