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FDA 510(k)

REDYPLATE DISPOSABLE LEG PLATE

K-Number: K901152 · 1990-04-04

ApplicantMedical Accessories, Inc.
Decision Date1990-04-04
Product CodeHGP
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

REDYPLATE DISPOSABLE LEG PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Accessories, Inc.. It received FDA 510(k) clearance on 1990-04-04 under 510(k) number K901152. The device is classified under product code HGP. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REDYPLATE DISPOSABLE LEG PLATE?

REDYPLATE DISPOSABLE LEG PLATE is a medical device that received FDA 510(k) clearance on 1990-04-04. The listed applicant is Medical Accessories, Inc.. The 510(k) number is K901152.

When did REDYPLATE DISPOSABLE LEG PLATE receive FDA 510(k) clearance?

REDYPLATE DISPOSABLE LEG PLATE received FDA 510(k) clearance on 1990-04-04, under 510(k) number K901152.

Who is the listed applicant for REDYPLATE DISPOSABLE LEG PLATE?

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

What is the FDA product code for REDYPLATE DISPOSABLE LEG PLATE?

The FDA product code for REDYPLATE DISPOSABLE LEG PLATE is HGP.

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 Medical Accessories, 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.

K920056POCKET SIZE FETAL HEART DETECTORK872057FETAL SCALP ELECTRODE

Related Devices (Code: HGP)

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.

K243291Goldtrace Fetal Spiral Electrode (FSE) (CNS000004)Neoventa Medical ABK030691FETAL SPIRAL ELECTRODE, MODEL FSE07000Clinical Innovations, Inc.K003458SOFT BEAT FETAL HEART RATE ELECTRODE MODEL SBT-7000Clinical Innovations, Inc.K943732LIFE TRACE FETAL SPIRAL ELECTRODE WITH MATERNAL REFERENCEGraphic Controls Corp.K910815CR SPIRAL ELECTRODENeward Enterprises, Inc.K911657FETAL SCALP SPIRAL ELECTRODEAdvanced Medical Systems, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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