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FDA 510(k)

RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM

K-Number: K904237 · 1991-05-09

ApplicantInnovative Medical Technologies, Inc.
Decision Date1991-05-09
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Technologies, Inc.. It received FDA 510(k) clearance on 1991-05-09 under 510(k) number K904237. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM?

RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM is a medical device that received FDA 510(k) clearance on 1991-05-09. The listed applicant is Innovative Medical Technologies, Inc.. The 510(k) number is K904237.

When did RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM receive FDA 510(k) clearance?

RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM received FDA 510(k) clearance on 1991-05-09, under 510(k) number K904237.

Who is the listed applicant for RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM?

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

What is the FDA product code for RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM?

The FDA product code for RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM is FPP.

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 Innovative Medical Technologies, 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.

K220458UltraFlo-R Push Button Blood Collection SetK123987IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SETK972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMK936087CARPAL BOXK854194IMT ULTRASONIC STRIDE MONITOR

Related Devices (Code: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, 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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