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FDA 510(k)

IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION)

K-Number: K063175 · 2008-03-14

ApplicantMedical Technology Systems, Inc.
Decision Date2008-03-14
Product CodeMOC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technology Systems, Inc.. It received FDA 510(k) clearance on 2008-03-14 under 510(k) number K063175. The device is classified under product code MOC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION)?

IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION) is a medical device that received FDA 510(k) clearance on 2008-03-14. The listed applicant is Medical Technology Systems, Inc.. The 510(k) number is K063175.

When did IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION) receive FDA 510(k) clearance?

IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION) received FDA 510(k) clearance on 2008-03-14, under 510(k) number K063175.

Who is the listed applicant for IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION)?

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

What is the FDA product code for IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION)?

The FDA product code for IPUP 200 (INTELLIGENT PRESSURE ULCER PREVENTION) is MOC.

Related Clinical Trials

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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Other records listing Medical Technology Systems, 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.

K854476KALMATE MODEL 3A

Related Devices (Code: MOC)

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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