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FDA 510(k)

SS102 DUAL CHANNEL SEP STIMULATOR

K-Number: K955257 · 1996-02-02

ApplicantAxon Systems, Inc.
Decision Date1996-02-02
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SS102 DUAL CHANNEL SEP STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Axon Systems, Inc.. It received FDA 510(k) clearance on 1996-02-02 under 510(k) number K955257. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SS102 DUAL CHANNEL SEP STIMULATOR?

SS102 DUAL CHANNEL SEP STIMULATOR is a medical device that received FDA 510(k) clearance on 1996-02-02. The listed applicant is Axon Systems, Inc.. The 510(k) number is K955257.

When did SS102 DUAL CHANNEL SEP STIMULATOR receive FDA 510(k) clearance?

SS102 DUAL CHANNEL SEP STIMULATOR received FDA 510(k) clearance on 1996-02-02, under 510(k) number K955257.

Who is the listed applicant for SS102 DUAL CHANNEL SEP STIMULATOR?

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

What is the FDA product code for SS102 DUAL CHANNEL SEP STIMULATOR?

The FDA product code for SS102 DUAL CHANNEL SEP STIMULATOR is GWF.

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Other records listing Axon Systems, 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.

K090838STIMULUS/DISSECTION INSTRUMENTSK062996DISPOSABLE MONOPOLAR AND BIPOLAR STIMULATOR PROBESK062198SUNSPOTS PRE-GELLED SURFACE ELECTRODESK061639ECLIPSE TCD NEUROVASCULAR WORKSTATION; ELCLIPSE NEUROLOGICAL WORKSTATION WITH TCD AND VASCULAR DOPPLER; CARDIOMONK061113ORTHOMONK050798ECLIPSE NEUROLOGICAL WORKSTATION

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Related Devices (Code: GWF)

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.

K263010ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpressinomed Medizintechnik GmbHK253301BraiN20® (BraiN20)Time IS Brain, S.L.K252842SafeOp 3: Neural Informatix SystemAlphatec Spine, Inc.K243982Nicolet EDXNatus Neurology IncorporatedK243495Natus Ultrapro S100 (982A0594)Natus Neurology IncorporatedK242345Delphi StimulatorQuantalx Neuroscience

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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