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FDA 510(k)

HYDRO-THERO PAD

K-Number: K841697 · 1984-05-09

ApplicantMaddak, Inc.
Decision Date1984-05-09
Product CodeIRT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HYDRO-THERO PAD is the device name listed in this FDA 510(k) record. The listed applicant is Maddak, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K841697. The device is classified under product code IRT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRO-THERO PAD?

HYDRO-THERO PAD is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Maddak, Inc.. The 510(k) number is K841697.

When did HYDRO-THERO PAD receive FDA 510(k) clearance?

HYDRO-THERO PAD received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841697.

Who is the listed applicant for HYDRO-THERO PAD?

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

What is the FDA product code for HYDRO-THERO PAD?

The FDA product code for HYDRO-THERO PAD is IRT.

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Other records listing Maddak, 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.

K841700WALK & ROLLK841698HEAT PACKK841695CRAWLERK841692PRONE STANDERK841693STANDING FRAMEK841691SPLIT SEAT POSITIONING CHAIR

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Related Devices (Code: IRT)

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.

K250047bite away twomibeTec GmbHK220514bite away neomibeTec GmbHK160943Bite AwayRiemser PharmaK111273FIR HEAT THERAPHY SYSYEMSShenzhen Anpan Technology Co., Ltd.K072534BIO-MAT 2000Richway Intl., Inc.K963887PT-PAC PORTABLE HEATING PADAnthony A. Chiurco

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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