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FDA 510(k)

NEOCUSSOR (MASSAGER, BATTERY) POWERED

K-Number: K855129 · 1986-01-23

ApplicantGeneral Physiotherapy, Inc.
Decision Date1986-01-23
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEOCUSSOR (MASSAGER, BATTERY) POWERED is the device name listed in this FDA 510(k) record. The listed applicant is General Physiotherapy, Inc.. It received FDA 510(k) clearance on 1986-01-23 under 510(k) number K855129. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOCUSSOR (MASSAGER, BATTERY) POWERED?

NEOCUSSOR (MASSAGER, BATTERY) POWERED is a medical device that received FDA 510(k) clearance on 1986-01-23. The listed applicant is General Physiotherapy, Inc.. The 510(k) number is K855129.

When did NEOCUSSOR (MASSAGER, BATTERY) POWERED receive FDA 510(k) clearance?

NEOCUSSOR (MASSAGER, BATTERY) POWERED received FDA 510(k) clearance on 1986-01-23, under 510(k) number K855129.

Who is the listed applicant for NEOCUSSOR (MASSAGER, BATTERY) POWERED?

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

What is the FDA product code for NEOCUSSOR (MASSAGER, BATTERY) POWERED?

The FDA product code for NEOCUSSOR (MASSAGER, BATTERY) POWERED is BYI.

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Other records listing General Physiotherapy, 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.

K870939VIBRACAREK863383FACIAL MASSAGER, BATTERY POWEREDK861834THERACUSHION MODEL 1000K853710THERACUSHIONK852944FLEXIMATIC MASSAGERK850047SANYO ELECTRONIC MUSCLE STIMULATORS

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Related Devices (Code: BYI)

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.

K252849AffloVest® Mobile Airway Clearance TherapyTactile MedicalK250860BreatheBand® (Model 1000)Exemplar Medical, LLCK242063LibAirty Airway Clearance SystemSynchrony Medical , Ltd.K240959Respiratory Muscle TrainerChongqing Moffy Innovation Technology Co., Ltd.K233441The Vest APX System (PVAPX1)Baxter Healthcare CorportationK222496Electromed SmartVest Airway Clearance SystemElectromed, Inc.

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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