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FDA 510(k)

MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL

K-Number: K042717 · 2004-11-05

Decision Date2004-11-05
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Analysis Systems, Inc.. It received FDA 510(k) clearance on 2004-11-05 under 510(k) number K042717. 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 MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL?

MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL is a medical device that received FDA 510(k) clearance on 2004-11-05. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K042717.

When did MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL receive FDA 510(k) clearance?

MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL received FDA 510(k) clearance on 2004-11-05, under 510(k) number K042717.

Who is the listed applicant for MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL?

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

What is the FDA product code for MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL?

The FDA product code for MAS, DADE AND LIQUID ASSAYED DIABETES CONTROL 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 Medical Analysis 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 107 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

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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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