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FDA 510(k)

HARE MODEL 2000 EZ LOADER MODEL 95555

K-Number: K962181 · 1996-08-01

ApplicantDyna Corp.
Decision Date1996-08-01
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HARE MODEL 2000 EZ LOADER MODEL 95555 is the device name listed in this FDA 510(k) record. The listed applicant is Dyna Corp.. It received FDA 510(k) clearance on 1996-08-01 under 510(k) number K962181. 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 HARE MODEL 2000 EZ LOADER MODEL 95555?

HARE MODEL 2000 EZ LOADER MODEL 95555 is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Dyna Corp.. The 510(k) number is K962181.

When did HARE MODEL 2000 EZ LOADER MODEL 95555 receive FDA 510(k) clearance?

HARE MODEL 2000 EZ LOADER MODEL 95555 received FDA 510(k) clearance on 1996-08-01, under 510(k) number K962181.

Who is the listed applicant for HARE MODEL 2000 EZ LOADER MODEL 95555?

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

What is the FDA product code for HARE MODEL 2000 EZ LOADER MODEL 95555?

The FDA product code for HARE MODEL 2000 EZ LOADER MODEL 95555 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 Dyna Corp. 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.

K972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)K902503HARE FOLDING BACK EMERGENCY STRETCHERK900670HARE EMERGENCY STRETCHERK900671HARE EMERGENCY STRETCHER WITH WHEELS

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.K961437WHEELED STRETCHERHill-Rom, Inc.K952447HILL-ROM AMBULATORY CARE PROCEDURAL 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.

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