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FDA 510(k)

NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM

K-Number: K070960 · 2007-07-11

Decision Date2007-07-11
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nova Biomedical Corp.. It received FDA 510(k) clearance on 2007-07-11 under 510(k) number K070960. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM?

NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM is a medical device that received FDA 510(k) clearance on 2007-07-11. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K070960.

When did NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM receive FDA 510(k) clearance?

NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM received FDA 510(k) clearance on 2007-07-11, under 510(k) number K070960.

Who is the listed applicant for NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM?

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

What is the FDA product code for NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM?

The FDA product code for NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM is CGA.

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 Nova Biomedical 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.

View all 89 devices →

Related Devices (Code: CGA)

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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