Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II

K-Number: K880545 · 1988-05-31

ApplicantStimwear
Decision Date1988-05-31
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II is the device name listed in this FDA 510(k) record. The listed applicant is Stimwear. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K880545. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II?

STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Stimwear. The 510(k) number is K880545.

When did STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II receive FDA 510(k) clearance?

STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II received FDA 510(k) clearance on 1988-05-31, under 510(k) number K880545.

Who is the listed applicant for STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II?

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

What is the FDA product code for STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II?

The FDA product code for STIMWEAR GARMENTS, SIGNAL I AND SIGNAL II is GXY.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: GXY)

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.

K262654Dexus Prosthetic System (MSL2, MSR2)Zhejiang Qiangnao Technology Co.,LtdK260578Ambu® NeurolineTM Cup MRI/CT (Models 72704/21US, 72704/23US, 72704/25US, 72704/27US) Ambu® NeurolineTM Cup MRI/CT-set (Models 72704/21-1010US, 72704/21-1010US, 72704/23-1010US, 72704/25-1010US, 72704/27-1010US) Ambu® NeurolineTM Cup MRI/CT-mini set (Models 72704/21-0301US, 72704/23-0301US, 72704/25-0301US, 72704/27-0301US)Ambu A/SK261442Charlotte ACC25 Surface Electrode Array; Charlotte ACC25 Reusable Surface Electrode ArrayCadwell Industries, Inc.K261522BioWave BioWrapsBiowave CorporationK253237Elde Medical Electrodes (T5/ 5 cm x 5cm electrode T10/ 5 cm x 10cm electrode)Elde Medikal Sanayi ve Ticaret Anonim SirketiK254183MR Conditional Cup ElectrodesTechnomed Europe

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.

↑