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FDA 510(k)

CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000

K-Number: K033358 · 2003-11-14

ApplicantSurgitech, Inc.
Decision Date2003-11-14
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Surgitech, Inc.. It received FDA 510(k) clearance on 2003-11-14 under 510(k) number K033358. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000?

CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000 is a medical device that received FDA 510(k) clearance on 2003-11-14. The listed applicant is Surgitech, Inc.. The 510(k) number is K033358.

When did CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000 receive FDA 510(k) clearance?

CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000 received FDA 510(k) clearance on 2003-11-14, under 510(k) number K033358.

Who is the listed applicant for CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000?

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

What is the FDA product code for CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000?

The FDA product code for CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000 is LIH.

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Other records listing Surgitech, 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.

K031576SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1

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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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