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FDA 510(k)

CURAMED 402

K-Number: K850573 · 1985-05-17

ApplicantFluidotherapy Corp.
Decision Date1985-05-17
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CURAMED 402 is the device name listed in this FDA 510(k) record. The listed applicant is Fluidotherapy Corp.. It received FDA 510(k) clearance on 1985-05-17 under 510(k) number K850573. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURAMED 402?

CURAMED 402 is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Fluidotherapy Corp.. The 510(k) number is K850573.

When did CURAMED 402 receive FDA 510(k) clearance?

CURAMED 402 received FDA 510(k) clearance on 1985-05-17, under 510(k) number K850573.

Who is the listed applicant for CURAMED 402?

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

What is the FDA product code for CURAMED 402?

The FDA product code for CURAMED 402 is IMJ.

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 Fluidotherapy Corp. 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.

K850640SONOPULS 434 ULTRASOUND THERAPY EQUIPMENTK832122ENRAF NONIVS2 CHANNEL EMG/TEMP. FEED

Related Devices (Code: IMJ)

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.

K252963BTL-899TTBTL Industries, Inc.K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLC

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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