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FDA 510(k)

ELECSYS DHEA-S CALCHECK 5

K-Number: K103402 · 2011-01-07

Decision Date2011-01-07
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECSYS DHEA-S CALCHECK 5 is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics. It received FDA 510(k) clearance on 2011-01-07 under 510(k) number K103402. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECSYS DHEA-S CALCHECK 5?

ELECSYS DHEA-S CALCHECK 5 is a medical device that received FDA 510(k) clearance on 2011-01-07. The listed applicant is Roche Diagnostics. The 510(k) number is K103402.

When did ELECSYS DHEA-S CALCHECK 5 receive FDA 510(k) clearance?

ELECSYS DHEA-S CALCHECK 5 received FDA 510(k) clearance on 2011-01-07, under 510(k) number K103402.

Who is the listed applicant for ELECSYS DHEA-S CALCHECK 5?

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

What is the FDA product code for ELECSYS DHEA-S CALCHECK 5?

The FDA product code for ELECSYS DHEA-S CALCHECK 5 is JJX.

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 Roche Diagnostics 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 164 devices →

Related Devices (Code: JJX)

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.

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