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FDA 510(k)

AIR PRESS MASSAGER

K-Number: K032505 · 2003-09-24

ApplicantTelebrands Corp
Decision Date2003-09-24
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AIR PRESS MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Telebrands Corp. It received FDA 510(k) clearance on 2003-09-24 under 510(k) number K032505. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR PRESS MASSAGER?

AIR PRESS MASSAGER is a medical device that received FDA 510(k) clearance on 2003-09-24. The listed applicant is Telebrands Corp. The 510(k) number is K032505.

When did AIR PRESS MASSAGER receive FDA 510(k) clearance?

AIR PRESS MASSAGER received FDA 510(k) clearance on 2003-09-24, under 510(k) number K032505.

Who is the listed applicant for AIR PRESS MASSAGER?

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

What is the FDA product code for AIR PRESS MASSAGER?

The FDA product code for AIR PRESS MASSAGER is IRP.

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Related Devices (Code: IRP)

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.

K260944ManaCold Compression SystemManamed, LLCK260529Air Compression Massager (HY-1165)Xiamen High Top Electronic Technology Co., Ltd.K260948Air Compression Massager (EP30B001 I)Wavepulse (Xiamen) Healthcare Technology Co., Ltd.K253919Cryo And Thermo Therapy SystemXiamen Weiyou Intelligent Technology Co., Ltd.K252396Cryo Sport 2.0 (AVA 501)Avanutri Equipamentos DE SaúdeK254200Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14)Wenzhou Lingfeng Electronic Technology Co., Ltd.

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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