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FDA 510(k)

STAODYN MAXIMA III

K-Number: K930865 · 1993-05-13

ApplicantStaodyne, Inc.
Decision Date1993-05-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STAODYN MAXIMA III is the device name listed in this FDA 510(k) record. The listed applicant is Staodyne, Inc.. It received FDA 510(k) clearance on 1993-05-13 under 510(k) number K930865. 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 STAODYN MAXIMA III?

STAODYN MAXIMA III is a medical device that received FDA 510(k) clearance on 1993-05-13. The listed applicant is Staodyne, Inc.. The 510(k) number is K930865.

When did STAODYN MAXIMA III receive FDA 510(k) clearance?

STAODYN MAXIMA III received FDA 510(k) clearance on 1993-05-13, under 510(k) number K930865.

Who is the listed applicant for STAODYN MAXIMA III?

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

What is the FDA product code for STAODYN MAXIMA III?

The FDA product code for STAODYN MAXIMA III is GZJ.

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Other records listing Staodyne, 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.

K952680VARAPULSE-2K941923STERILE TREATMENT ELECTRODEK931925TPK CUTANEOUS ELECTRODEK926510STAODYN EMS+2K931424MAXIMA IK925898MODEL 19 STIMULATOR, NERVE, TRANSCUTANEOUS

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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

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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