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FDA 510(k)

FRUCTOSAMINE, MODEL FR 106-01

K-Number: K991246 · 1999-12-16

ApplicantA.P. Total Care, Inc.
Decision Date1999-12-16
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FRUCTOSAMINE, MODEL FR 106-01 is the device name listed in this FDA 510(k) record. The listed applicant is A.P. Total Care, Inc.. It received FDA 510(k) clearance on 1999-12-16 under 510(k) number K991246. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRUCTOSAMINE, MODEL FR 106-01?

FRUCTOSAMINE, MODEL FR 106-01 is a medical device that received FDA 510(k) clearance on 1999-12-16. The listed applicant is A.P. Total Care, Inc.. The 510(k) number is K991246.

When did FRUCTOSAMINE, MODEL FR 106-01 receive FDA 510(k) clearance?

FRUCTOSAMINE, MODEL FR 106-01 received FDA 510(k) clearance on 1999-12-16, under 510(k) number K991246.

Who is the listed applicant for FRUCTOSAMINE, MODEL FR 106-01?

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

What is the FDA product code for FRUCTOSAMINE, MODEL FR 106-01?

The FDA product code for FRUCTOSAMINE, MODEL FR 106-01 is LCP.

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Other records listing A.P. Total Care, Inc. 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.

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Related Devices (Code: LCP)

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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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