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FDA 510(k)

WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS

K-Number: K954577 · 1997-05-09

ApplicantC.A.I. Industries Corp.
Decision Date1997-05-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is C.A.I. Industries Corp.. It received FDA 510(k) clearance on 1997-05-09 under 510(k) number K954577. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS?

WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS is a medical device that received FDA 510(k) clearance on 1997-05-09. The listed applicant is C.A.I. Industries Corp.. The 510(k) number is K954577.

When did WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS receive FDA 510(k) clearance?

WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS received FDA 510(k) clearance on 1997-05-09, under 510(k) number K954577.

Who is the listed applicant for WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS?

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

What is the FDA product code for WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS?

The FDA product code for WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS is ILY.

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 C.A.I. Industries 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.

K041652ACUPUNCTURE NEEDLESK970574ACUPUNCTURE NEEDLES

Related Devices (Code: ILY)

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.

K253965CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.)Wuhan PHOMED Technology Company , Ltd.K242755Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B)Gigaalaser Company , Ltd.K231997SIRONA 100 Therapy Laser System (OEM's Model EVANLAS)Cure Point Therapeutics, Inc.K223642LED Lip Perfector, model: ZC-05Light Tree Ventures Europe B.V.K221189OLIZ LTB-1000ALtbio Co., Ltd.K213524CytonPro-5000Cytonsys, Inc.

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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