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FDA 510(k)

CARE IFC PLUS

K-Number: K020516 · 2002-05-16

ApplicantCare Rehab, Inc.
Decision Date2002-05-16
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CARE IFC PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Care Rehab, Inc.. It received FDA 510(k) clearance on 2002-05-16 under 510(k) number K020516. 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 CARE IFC PLUS?

CARE IFC PLUS is a medical device that received FDA 510(k) clearance on 2002-05-16. The listed applicant is Care Rehab, Inc.. The 510(k) number is K020516.

When did CARE IFC PLUS receive FDA 510(k) clearance?

CARE IFC PLUS received FDA 510(k) clearance on 2002-05-16, under 510(k) number K020516.

Who is the listed applicant for CARE IFC PLUS?

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

What is the FDA product code for CARE IFC PLUS?

The FDA product code for CARE IFC PLUS is LIH.

Other records listing Care Rehab, 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.

K021905CLASSIC NMSK020437CLASSIC TENSK984025CARE TENS

Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

Official Source

View on FDA Database →

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

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