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FDA 510(k)

S-610 & 2-628 WHEELED SHOWER STRETCHERS

K-Number: K933060 · 1994-02-04

ApplicantThe Anthros Medical Group
Decision Date1994-02-04
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

S-610 & 2-628 WHEELED SHOWER STRETCHERS is the device name listed in this FDA 510(k) record. The listed applicant is The Anthros Medical Group. It received FDA 510(k) clearance on 1994-02-04 under 510(k) number K933060. 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 S-610 & 2-628 WHEELED SHOWER STRETCHERS?

S-610 & 2-628 WHEELED SHOWER STRETCHERS is a medical device that received FDA 510(k) clearance on 1994-02-04. The listed applicant is The Anthros Medical Group. The 510(k) number is K933060.

When did S-610 & 2-628 WHEELED SHOWER STRETCHERS receive FDA 510(k) clearance?

S-610 & 2-628 WHEELED SHOWER STRETCHERS received FDA 510(k) clearance on 1994-02-04, under 510(k) number K933060.

Who is the listed applicant for S-610 & 2-628 WHEELED SHOWER STRETCHERS?

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

What is the FDA product code for S-610 & 2-628 WHEELED SHOWER STRETCHERS?

The FDA product code for S-610 & 2-628 WHEELED SHOWER STRETCHERS 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 The Anthros Medical Group 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.

K921752AMBULATOR

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

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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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