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FDA 510(k)

GLUCOSE HK PROCEDURE

K-Number: K861653 · 1986-05-23

ApplicantData Medical Associates, Inc.
Decision Date1986-05-23
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSE HK PROCEDURE is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1986-05-23 under 510(k) number K861653. 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 GLUCOSE HK PROCEDURE?

GLUCOSE HK PROCEDURE is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K861653.

When did GLUCOSE HK PROCEDURE receive FDA 510(k) clearance?

GLUCOSE HK PROCEDURE received FDA 510(k) clearance on 1986-05-23, under 510(k) number K861653.

Who is the listed applicant for GLUCOSE HK PROCEDURE?

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

What is the FDA product code for GLUCOSE HK PROCEDURE?

The FDA product code for GLUCOSE HK PROCEDURE is CGA.

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Other records listing Data Medical Associates, Inc. as applicant

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Related Devices (Code: CGA)

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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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