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FDA 510(k)

SONICAID MODEL TEAM FECG IUP

K-Number: K930714 · 1995-08-24

ApplicantOxford Instruments, Plc.
Decision Date1995-08-24
Product CodeHEL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SONICAID MODEL TEAM FECG IUP is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Instruments, Plc.. It received FDA 510(k) clearance on 1995-08-24 under 510(k) number K930714. The device is classified under product code HEL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONICAID MODEL TEAM FECG IUP?

SONICAID MODEL TEAM FECG IUP is a medical device that received FDA 510(k) clearance on 1995-08-24. The listed applicant is Oxford Instruments, Plc.. The 510(k) number is K930714.

When did SONICAID MODEL TEAM FECG IUP receive FDA 510(k) clearance?

SONICAID MODEL TEAM FECG IUP received FDA 510(k) clearance on 1995-08-24, under 510(k) number K930714.

Who is the listed applicant for SONICAID MODEL TEAM FECG IUP?

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

What is the FDA product code for SONICAID MODEL TEAM FECG IUP?

The FDA product code for SONICAID MODEL TEAM FECG IUP is HEL.

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 Oxford Instruments, Plc. 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.

K981405SYNERGY LTK961636MEDILOG VISIONK961642MEDILOG MR95K933816SONICAID MODEL P110 FETAL HEAR DETECTOR

Related Devices (Code: HEL)

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.

K003876US SENSOR #CG-930P; TOCO SENSOR CG-940PCard Guard Scientific Survival , Ltd.K010920TRANSDUCERS FOR FETAL ULTRASONIC AND TOKODYNAMOMETER MONITORINGMedical Cables, Inc.K982651COROMETRICS MODEL 5700 AND 2264 WATERTIGHT TRANSDUCERCorometrics Medical Systems, Inc.K971240ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M006Alexander Mfg. Co.K933816SONICAID MODEL P110 FETAL HEAR DETECTOROxford Instruments, Plc.K780035MINIVISORMetrix Teknika, 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.

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