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FDA 510(k)

MAPS 10000

K-Number: K992560 · 1999-10-29

Decision Date1999-10-29
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAPS 10000 is the device name listed in this FDA 510(k) record. The listed applicant is Web Link Medical. It received FDA 510(k) clearance on 1999-10-29 under 510(k) number K992560. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAPS 10000?

MAPS 10000 is a medical device that received FDA 510(k) clearance on 1999-10-29. The listed applicant is Web Link Medical. The 510(k) number is K992560.

When did MAPS 10000 receive FDA 510(k) clearance?

MAPS 10000 received FDA 510(k) clearance on 1999-10-29, under 510(k) number K992560.

Who is the listed applicant for MAPS 10000?

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

What is the FDA product code for MAPS 10000?

The FDA product code for MAPS 10000 is KPS.

Related Devices (Code: KPS)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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