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FDA 510(k)

THERATRONIC STIMULATOR

K-Number: K820782 · 1982-06-03

ApplicantTheratronics, Inc.
Decision Date1982-06-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THERATRONIC STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Theratronics, Inc.. It received FDA 510(k) clearance on 1982-06-03 under 510(k) number K820782. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERATRONIC STIMULATOR?

THERATRONIC STIMULATOR is a medical device that received FDA 510(k) clearance on 1982-06-03. The listed applicant is Theratronics, Inc.. The 510(k) number is K820782.

When did THERATRONIC STIMULATOR receive FDA 510(k) clearance?

THERATRONIC STIMULATOR received FDA 510(k) clearance on 1982-06-03, under 510(k) number K820782.

Who is the listed applicant for THERATRONIC STIMULATOR?

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

What is the FDA product code for THERATRONIC STIMULATOR?

The FDA product code for THERATRONIC STIMULATOR is IPF.

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Other records listing Theratronics, 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.

K983917THERATRON ELITEK970236THERAPLAN PLUS VERSION 1.2K964606THERATRON 780EK964607THERATON 1000EK954679THERAPLAN PLUSK940237THERAPLAN V05B/ TP-11 V09B

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Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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