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FDA 510(k)

MATTRESSES, CONDUCTIVE & COVERS

K-Number: K780033 · 1978-02-21

ApplicantChase Mfg. Co.
Decision Date1978-02-21
Product CodeFMW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MATTRESSES, CONDUCTIVE & COVERS is the device name listed in this FDA 510(k) record. The listed applicant is Chase Mfg. Co.. It received FDA 510(k) clearance on 1978-02-21 under 510(k) number K780033. The device is classified under product code FMW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATTRESSES, CONDUCTIVE & COVERS?

MATTRESSES, CONDUCTIVE & COVERS is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Chase Mfg. Co.. The 510(k) number is K780033.

When did MATTRESSES, CONDUCTIVE & COVERS receive FDA 510(k) clearance?

MATTRESSES, CONDUCTIVE & COVERS received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780033.

Who is the listed applicant for MATTRESSES, CONDUCTIVE & COVERS?

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

What is the FDA product code for MATTRESSES, CONDUCTIVE & COVERS?

The FDA product code for MATTRESSES, CONDUCTIVE & COVERS is FMW.

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Other records listing Chase Mfg. Co. 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.

K791513ADAMCO DUST COVERK790993INSTANT HOT & COLD PACKSK790644SUBMAXK771792ENEMA SETK771791NEEDLE COUNTINGK770900CAST BRWM, FRACTURE

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Related Devices (Code: FMW)

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.

K152884DermaTherapy Bed LinensPrecision Fabrics Group, Inc.K061242DERMATHERAPY, MODEL 22216Precision Fabrics Group, Inc.K001003Z-NETDemite LimitedK992702EVENT ALLERGEN BARRIERS, EVENT MATTRESS ENCASING, EVENT DUVET ENCASING, EVENT PILLOW ENCASING, EVENT BEDDING SYSTEMAllergy DirectK940327INTERVENT ALLERGEN EXCLUSION TECHNOLOGY, INTERVENT BEDDING SYSTEM, INTERVENT MATTRESS INTERLINER, INTERVIEW PILLOWW. L. Gore & Associates, Inc.K935220CORE PREVENT MATTRESS MODIFICATIONPaladin Medical, 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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