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FDA 510(k)

THE PAIN PILOT (A.K.A PAIN PILOT)

K-Number: K120500 · 2012-08-20

ApplicantHollywog, LLC
Decision Date2012-08-20
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE PAIN PILOT (A.K.A PAIN PILOT) is the device name listed in this FDA 510(k) record. The listed applicant is Hollywog, LLC. It received FDA 510(k) clearance on 2012-08-20 under 510(k) number K120500. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PAIN PILOT (A.K.A PAIN PILOT)?

THE PAIN PILOT (A.K.A PAIN PILOT) is a medical device that received FDA 510(k) clearance on 2012-08-20. The listed applicant is Hollywog, LLC. The 510(k) number is K120500.

When did THE PAIN PILOT (A.K.A PAIN PILOT) receive FDA 510(k) clearance?

THE PAIN PILOT (A.K.A PAIN PILOT) received FDA 510(k) clearance on 2012-08-20, under 510(k) number K120500.

Who is the listed applicant for THE PAIN PILOT (A.K.A PAIN PILOT)?

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

What is the FDA product code for THE PAIN PILOT (A.K.A PAIN PILOT)?

The FDA product code for THE PAIN PILOT (A.K.A PAIN PILOT) is NUH.

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Other records listing Hollywog, LLC 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.

K171599WiTouch Pro, WiTouch, NeubacK120398WITOUCH PRO

Related Devices (Code: NUH)

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.

K261131Electrical Muscle Stimulator (AST-105DJ, AST-105EJ, AST- 105BJ, AST-105GJ, AST-303J, AST-309J, AST-310J;AST-300Q, AST-300Q-A, AST-500B; AST-500G, AST-500F; AST-500N; AST- 500C, AST- 500K, AST-500A; AST-300E, AST-500M, AST- 500U, AST- 500D; AST- 500E.)Shenzhen Osto Medical Technology Co.,LtdK260412TENS 7000 Rechargeable 4 Channel (TENS 7000H)Shenzhen Dongdixin Technology Co., Ltd.K260425TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)Hivox Biotek, Inc.K253896TENS/EMS device (GUSE01)Globalcare Medical Technology Co., Ltd.K253305TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034)Shenzhen Jiantuo Electronics Co., Ltd.K251958VEINOPLUS BackDynapulse Medical

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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