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)

DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)

K-Number: K972528 · 1997-07-28

ApplicantDyna Corp.
Decision Date1997-07-28
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) is the device name listed in this FDA 510(k) record. The listed applicant is Dyna Corp.. It received FDA 510(k) clearance on 1997-07-28 under 510(k) number K972528. 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 DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)?

DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) is a medical device that received FDA 510(k) clearance on 1997-07-28. The listed applicant is Dyna Corp.. The 510(k) number is K972528.

When did DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) receive FDA 510(k) clearance?

DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) received FDA 510(k) clearance on 1997-07-28, under 510(k) number K972528.

Who is the listed applicant for DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)?

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 DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)?

The FDA product code for DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) 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.

K962181HARE MODEL 2000 EZ LOADER MODEL 95555K902503HARE 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, LLCK955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.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.

↑