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)

STRYKER I.V. CADDY ACCESSORY DEVICE

K-Number: K920704 · 1992-03-23

ApplicantStryker Medical
Decision Date1992-03-23
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER I.V. CADDY ACCESSORY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 1992-03-23 under 510(k) number K920704. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER I.V. CADDY ACCESSORY DEVICE?

STRYKER I.V. CADDY ACCESSORY DEVICE is a medical device that received FDA 510(k) clearance on 1992-03-23. The listed applicant is Stryker Medical. The 510(k) number is K920704.

When did STRYKER I.V. CADDY ACCESSORY DEVICE receive FDA 510(k) clearance?

STRYKER I.V. CADDY ACCESSORY DEVICE received FDA 510(k) clearance on 1992-03-23, under 510(k) number K920704.

Who is the listed applicant for STRYKER I.V. CADDY ACCESSORY DEVICE?

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

What is the FDA product code for STRYKER I.V. CADDY ACCESSORY DEVICE?

The FDA product code for STRYKER I.V. CADDY ACCESSORY DEVICE is FPO.

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 Stryker Medical 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.

K222818Xpedition ™ Powered Stair Chair (625700000000)K180834Altrix Precision Temperature Management SystemK171149Altrix Temperature Management WrapsK152266Altrix Precision Temperature Management SystemK113598POWER-LOAD COT FASTENER SYSTEMK946149STRYKER AGILITY INTENSIVE CARE BED

View all 14 devices →

Related Devices (Code: FPO)

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.

K113598POWER-LOAD COT FASTENER SYSTEMStryker MedicalK072598IRSG I-MOVER FOR BEDSInternational Retail Services Group, LLCK972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)Dyna Corp.K955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.K961437WHEELED STRETCHERHill-Rom, 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.

↑