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)

CITADEL REFERENCE ELECTRODE

K-Number: K770477 · 1977-03-30

ApplicantSherwood Medical Industries
Decision Date1977-03-30
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CITADEL REFERENCE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770477. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CITADEL REFERENCE ELECTRODE?

CITADEL REFERENCE ELECTRODE is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Sherwood Medical Industries. The 510(k) number is K770477.

When did CITADEL REFERENCE ELECTRODE receive FDA 510(k) clearance?

CITADEL REFERENCE ELECTRODE received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770477.

Who is the listed applicant for CITADEL REFERENCE ELECTRODE?

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

What is the FDA product code for CITADEL REFERENCE ELECTRODE?

The FDA product code for CITADEL REFERENCE ELECTRODE is DRF.

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

Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

View all 62 devices →

Related Devices (Code: DRF)

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.

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific CorporationK240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific CorporationK233900Nordica PV Cryo Mapping CatheterSynaptic Medical CorporationK233397Cosine-10TM Diagnostic CatheterMedtronic, 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.

↑