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FDA 510(k)

PREFTEST PROFESSIONAL SUITE

K-Number: K052929 · 2006-04-26

ApplicantLimestone Technologies, Inc.
Decision Date2006-04-26
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

PREFTEST PROFESSIONAL SUITE is the device name listed in this FDA 510(k) record. The listed applicant is Limestone Technologies, Inc.. It received FDA 510(k) clearance on 2006-04-26 under 510(k) number K052929. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREFTEST PROFESSIONAL SUITE?

PREFTEST PROFESSIONAL SUITE is a medical device that received FDA 510(k) clearance on 2006-04-26. The listed applicant is Limestone Technologies, Inc.. The 510(k) number is K052929.

When did PREFTEST PROFESSIONAL SUITE receive FDA 510(k) clearance?

PREFTEST PROFESSIONAL SUITE received FDA 510(k) clearance on 2006-04-26, under 510(k) number K052929.

Who is the listed applicant for PREFTEST PROFESSIONAL SUITE?

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

What is the FDA product code for PREFTEST PROFESSIONAL SUITE?

The FDA product code for PREFTEST PROFESSIONAL SUITE is LIL.

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Related Devices (Code: LIL)

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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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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