FDA 510(k)

NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN

K-Number: K930498 · 1994-12-12

Decision Date1994-12-12

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN is the device name listed in this FDA 510(k) record. The listed applicant is Neuromed, Inc.. It received FDA 510(k) clearance on 1994-12-12 under 510(k) number K930498. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN?

NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN is a medical device that received FDA 510(k) clearance on 1994-12-12. The listed applicant is Neuromed, Inc.. The 510(k) number is K930498.

When did NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN receive FDA 510(k) clearance?

NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN received FDA 510(k) clearance on 1994-12-12, under 510(k) number K930498.

Who is the listed applicant for NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN?

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

What is the FDA product code for NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN?

The FDA product code for NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN is GZB.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Neuromed, Inc. as applicant

K960728ONE STEP CONNECT LEADS (QUATTRODE, OCTRODE, CERVITRODE)K930536NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC K930242INTRODE INT-8 K921319NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30 K905596NEUROMED OCTRODE MODEL MNR-88B/88C NEUROSTIM SYST K905255NEUROMED MODEL 1992 LS LAMITRODE LEAD

View all 15 devices →

Related Devices (Code: GZB)

K233801Nalu Neurostimulation System for Spinal Cord Stimulation; Nalu Neurostimulation System for Peripheral Nerve StimulationBoston Scientific Neuromodulation K221376Nalu Neurostimulation SystemBoston Scientific Neuromodulation K203547Nalu Neurostimulation SystemBoston Scientific Neuromodulation K202274Nalu Neurostimulation Kit (lnte:gmted 40 em: Single 8/Dual 8), Nalu Neurostimulation Kit (Ported, 2 em: Single 8/Dual8), Dual 8 Ported Nalu Implantable Pulse Generator with 40 ern Kil, 40 cm/ 60 cm/60 em TrialJExtension Lead Kits, Patient Kits and miscellaneous replacement kitsBoston Scientific Neuromodulation K201618Nalu Neurostimulation SCS systemBoston Scientific Neuromodulation K191466SandShark Injectable Anchor (SIA) SystemStimwave Technologies, Inc.

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.