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FDA 510(k)

INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS

K-Number: K060014 · 2006-04-03

ApplicantIntelifuse, Inc.
Decision Date2006-04-03
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS is the device name listed in this FDA 510(k) record. The listed applicant is Intelifuse, Inc.. It received FDA 510(k) clearance on 2006-04-03 under 510(k) number K060014. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS?

INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS is a medical device that received FDA 510(k) clearance on 2006-04-03. The listed applicant is Intelifuse, Inc.. The 510(k) number is K060014.

When did INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS receive FDA 510(k) clearance?

INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS received FDA 510(k) clearance on 2006-04-03, under 510(k) number K060014.

Who is the listed applicant for INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS?

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

What is the FDA product code for INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS?

The FDA product code for INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS is JDR.

Related Clinical Trials

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Other records listing Intelifuse, 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.

K051408INTELIFUSE, INC. WARM SYSTEM WITH STIMULINKS

Related Devices (Code: JDR)

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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