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FDA 510(k)

GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK

K-Number: K081403 · 2008-07-25

ApplicantBionostics, Inc.
Decision Date2008-07-25
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK is the device name listed in this FDA 510(k) record. The listed applicant is Bionostics, Inc.. It received FDA 510(k) clearance on 2008-07-25 under 510(k) number K081403. 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 GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK?

GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK is a medical device that received FDA 510(k) clearance on 2008-07-25. The listed applicant is Bionostics, Inc.. The 510(k) number is K081403.

When did GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK receive FDA 510(k) clearance?

GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK received FDA 510(k) clearance on 2008-07-25, under 510(k) number K081403.

Who is the listed applicant for GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK?

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

What is the FDA product code for GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK?

The FDA product code for GLUCOSE METER-CHECK CONTROL SOLUTION FOR ROCHE ACCU-CHEK is JJX.

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Other records listing Bionostics, Inc. as applicant

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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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