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FDA 510(k)

MULTIPLE

K-Number: K833259 · 1984-04-02

ApplicantSun House Products Co.
Decision Date1984-04-02
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTIPLE is the device name listed in this FDA 510(k) record. The listed applicant is Sun House Products Co.. It received FDA 510(k) clearance on 1984-04-02 under 510(k) number K833259. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE?

MULTIPLE is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Sun House Products Co.. The 510(k) number is K833259.

When did MULTIPLE receive FDA 510(k) clearance?

MULTIPLE received FDA 510(k) clearance on 1984-04-02, under 510(k) number K833259.

Who is the listed applicant for MULTIPLE?

The FDA 510(k) record lists Sun House Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE?

The FDA product code for MULTIPLE is HQG.

Related Clinical Trials

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Related PubMed Literature

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.

PMID: 42290427Reliability and Consistency Analysis of Multiple Instruments for Scoliosis Screening in Adolescent Males: A Comparative Study of Instrument Accuracy.Studies in health technology and informatics ()PMID: 30115367The multiple arrhythmia dataset evaluation database (M.A.D.A.E.).Journal of electrocardiology ()

Related Devices (Code: HQG)

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.

K935919SUNGLASSESJa-Ru, Inc.K9207950R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEXOptical Radiation Corp.K900091MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOROnufryk Low Vision Ent.K884360SEIKO P-6 PROGRESSIVE SPECTACLE LENSESSeiko Corp.K882814NEOLENS PRESCRIPTION SPECTACLE LENSNeolens, Inc.K882308CR-39 PLASTIC LENSES FOR EYEGLASSESAutomated Lens System

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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