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FDA 510(k)

DIAL-AWAY PAIN

K-Number: K904457 · 1991-04-03

ApplicantR.F.P., Inc.
Decision Date1991-04-03
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIAL-AWAY PAIN is the device name listed in this FDA 510(k) record. The listed applicant is R.F.P., Inc.. It received FDA 510(k) clearance on 1991-04-03 under 510(k) number K904457. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAL-AWAY PAIN?

DIAL-AWAY PAIN is a medical device that received FDA 510(k) clearance on 1991-04-03. The listed applicant is R.F.P., Inc.. The 510(k) number is K904457.

When did DIAL-AWAY PAIN receive FDA 510(k) clearance?

DIAL-AWAY PAIN received FDA 510(k) clearance on 1991-04-03, under 510(k) number K904457.

Who is the listed applicant for DIAL-AWAY PAIN?

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

What is the FDA product code for DIAL-AWAY PAIN?

The FDA product code for DIAL-AWAY PAIN is GZJ.

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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