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FDA 510(k)

LOAD SENTINEL II, TRANS. ELEC. NERVE

K-Number: K802779 · 1980-12-10

ApplicantPowers Medical Systmes
Decision Date1980-12-10
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LOAD SENTINEL II, TRANS. ELEC. NERVE is the device name listed in this FDA 510(k) record. The listed applicant is Powers Medical Systmes. It received FDA 510(k) clearance on 1980-12-10 under 510(k) number K802779. 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 LOAD SENTINEL II, TRANS. ELEC. NERVE?

LOAD SENTINEL II, TRANS. ELEC. NERVE is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Powers Medical Systmes. The 510(k) number is K802779.

When did LOAD SENTINEL II, TRANS. ELEC. NERVE receive FDA 510(k) clearance?

LOAD SENTINEL II, TRANS. ELEC. NERVE received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802779.

Who is the listed applicant for LOAD SENTINEL II, TRANS. ELEC. NERVE?

The FDA 510(k) record lists Powers Medical Systmes as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOAD SENTINEL II, TRANS. ELEC. NERVE?

The FDA product code for LOAD SENTINEL II, TRANS. ELEC. NERVE is GZJ.

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Other records listing Powers Medical Systmes 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.

K811758ACCU-CHEK TRANS-TELEPHONIC PACEMAKER TRK801022ULTRA-CHEK PACEMAKER MONITOR

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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