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FDA 510(k)

GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER

K-Number: K971276 · 1997-06-16

ApplicantBayer Corp.
Decision Date1997-06-16
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER is the device name listed in this FDA 510(k) record. The listed applicant is Bayer Corp.. It received FDA 510(k) clearance on 1997-06-16 under 510(k) number K971276. The device is classified under product code CFR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER?

GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER is a medical device that received FDA 510(k) clearance on 1997-06-16. The listed applicant is Bayer Corp.. The 510(k) number is K971276.

When did GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER receive FDA 510(k) clearance?

GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER received FDA 510(k) clearance on 1997-06-16, under 510(k) number K971276.

Who is the listed applicant for GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER?

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

What is the FDA product code for GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER?

The FDA product code for GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER is CFR.

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Other records listing Bayer 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.

K024062ASCENSIA BREEZE BLOOD GLUCOSE METERK023944BAYER DIAGNOSTICS CLINITEST PREGNANCY TESTK024017BAYER ADVIA CENTAUR HER-2/NEU ASSAYK024234ASCENSIA GLUCOFACTS; ASCENSIA GLUCOFACTS PROFESSIONALK022288COMPLEXED PROSTATE SPECIFIC ANTIGEN (CPSA) ASSAY FOR THE BAYER ADVIA INTEGRATED MODULE SYSTEMK023584ASCENSIA DEX 2 DIABETES CARE SYSTEM

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Related Devices (Code: CFR)

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.

K253490Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutionsRoche DiagnosticsK252357Glucose2Abbott IrelandK220134cobas pure integrated solutions, Glucose HK Gen.3, ISE indirect Na for Gen.2, ONLINE DAT Methadone II, Elecsys TSHRoche DiagnosticsK191899Glucose HK Gen.3, ISE indirect Na for Gen.2, Elecsys TSH, cobas pro integrated solutionsRoche DiagnosticsK170316ALINITY C GLUCOSE REAGENT KIT, ALINITY C SYSTEMAbbott LaboratoriesK153644ELITech Clinical Systems GLUCOSE HK SL, ELITech Clinical Systems ELICAL 2, ELITech Clinical Systems ELITROL I and ELITROL IIElitechgroup

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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