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FDA 510(k)

GLUCOSCAN CONTROLS

K-Number: K822698 · 1982-09-30

ApplicantLifescan, Inc.
Decision Date1982-09-30
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSCAN CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Lifescan, Inc.. It received FDA 510(k) clearance on 1982-09-30 under 510(k) number K822698. 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 GLUCOSCAN CONTROLS?

GLUCOSCAN CONTROLS is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Lifescan, Inc.. The 510(k) number is K822698.

When did GLUCOSCAN CONTROLS receive FDA 510(k) clearance?

GLUCOSCAN CONTROLS received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822698.

Who is the listed applicant for GLUCOSCAN CONTROLS?

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

What is the FDA product code for GLUCOSCAN CONTROLS?

The FDA product code for GLUCOSCAN CONTROLS is JJX.

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Other records listing Lifescan, Inc. as applicant

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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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