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FDA 510(k)

DIAGEM DIGITAL BLOOD GLUCOSE MONITOR

K-Number: K841648 · 1984-10-11

ApplicantForward Medical Supplies
Decision Date1984-10-11
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIAGEM DIGITAL BLOOD GLUCOSE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Forward Medical Supplies. It received FDA 510(k) clearance on 1984-10-11 under 510(k) number K841648. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGEM DIGITAL BLOOD GLUCOSE MONITOR?

DIAGEM DIGITAL BLOOD GLUCOSE MONITOR is a medical device that received FDA 510(k) clearance on 1984-10-11. The listed applicant is Forward Medical Supplies. The 510(k) number is K841648.

When did DIAGEM DIGITAL BLOOD GLUCOSE MONITOR receive FDA 510(k) clearance?

DIAGEM DIGITAL BLOOD GLUCOSE MONITOR received FDA 510(k) clearance on 1984-10-11, under 510(k) number K841648.

Who is the listed applicant for DIAGEM DIGITAL BLOOD GLUCOSE MONITOR?

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

What is the FDA product code for DIAGEM DIGITAL BLOOD GLUCOSE MONITOR?

The FDA product code for DIAGEM DIGITAL BLOOD GLUCOSE MONITOR is JJQ.

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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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