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FDA 510(k)

ARP POV SPORT

K-Number: K093999 · 2010-08-10

ApplicantArp Manufacturing, Inc.
Decision Date2010-08-10
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARP POV SPORT is the device name listed in this FDA 510(k) record. The listed applicant is Arp Manufacturing, Inc.. It received FDA 510(k) clearance on 2010-08-10 under 510(k) number K093999. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARP POV SPORT?

ARP POV SPORT is a medical device that received FDA 510(k) clearance on 2010-08-10. The listed applicant is Arp Manufacturing, Inc.. The 510(k) number is K093999.

When did ARP POV SPORT receive FDA 510(k) clearance?

ARP POV SPORT received FDA 510(k) clearance on 2010-08-10, under 510(k) number K093999.

Who is the listed applicant for ARP POV SPORT?

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

What is the FDA product code for ARP POV SPORT?

The FDA product code for ARP POV SPORT is NGX.

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Other records listing Arp Manufacturing, 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.

K093259ARP RX100

Related Devices (Code: NGX)

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.

K253790High Intensity Focused Electromagnetic Stimulation Device (FE60)Beijing Winkonlaser Technology LimitedK253926DiacoreShenB Co., Ltd.K253636Zionic Pro Max (EMS)Termosalud S.L.K253408CoolToneZimmer Medizinsysteme GmbHK252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)Guangzhou Longest Medical Technology Co., Ltd.K253478Motive™ Muscle Stimulator for Lower Back (OT01-1003)Motive Health, 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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