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FDA 510(k)

MODEL 792 CONVERGE, MODEL 793 VISION 2000

K-Number: K945431 · 1995-01-25

ApplicantHausted, Inc.
Decision Date1995-01-25
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 792 CONVERGE, MODEL 793 VISION 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Hausted, Inc.. It received FDA 510(k) clearance on 1995-01-25 under 510(k) number K945431. 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 MODEL 792 CONVERGE, MODEL 793 VISION 2000?

MODEL 792 CONVERGE, MODEL 793 VISION 2000 is a medical device that received FDA 510(k) clearance on 1995-01-25. The listed applicant is Hausted, Inc.. The 510(k) number is K945431.

When did MODEL 792 CONVERGE, MODEL 793 VISION 2000 receive FDA 510(k) clearance?

MODEL 792 CONVERGE, MODEL 793 VISION 2000 received FDA 510(k) clearance on 1995-01-25, under 510(k) number K945431.

Who is the listed applicant for MODEL 792 CONVERGE, MODEL 793 VISION 2000?

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

What is the FDA product code for MODEL 792 CONVERGE, MODEL 793 VISION 2000?

The FDA product code for MODEL 792 CONVERGE, MODEL 793 VISION 2000 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.

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Other records listing Hausted, 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.

K943969MODEL 578 MOBILE SURGICAL STRETCHER

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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