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FDA 510(k)

ECHO PULSE BURST

K-Number: K842414 · 1984-07-27

ApplicantRabar, Inc.
Decision Date1984-07-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ECHO PULSE BURST is the device name listed in this FDA 510(k) record. The listed applicant is Rabar, Inc.. It received FDA 510(k) clearance on 1984-07-27 under 510(k) number K842414. 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 ECHO PULSE BURST?

ECHO PULSE BURST is a medical device that received FDA 510(k) clearance on 1984-07-27. The listed applicant is Rabar, Inc.. The 510(k) number is K842414.

When did ECHO PULSE BURST receive FDA 510(k) clearance?

ECHO PULSE BURST received FDA 510(k) clearance on 1984-07-27, under 510(k) number K842414.

Who is the listed applicant for ECHO PULSE BURST?

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

What is the FDA product code for ECHO PULSE BURST?

The FDA product code for ECHO PULSE BURST is GZJ.

Related Clinical Trials

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.

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Other records listing Rabar, 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.

K844017MICROTENS 7757 T.E.N.S. STIMULATORK821736ECHO-PULSE KM555

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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