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FDA 510(k)

MATTRESS COVER, ANTI-MICROBIAL

K-Number: K832483 · 1984-02-04

ApplicantAmerican Threshold Industries, Inc.
Decision Date1984-02-04
Product CodeFMW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MATTRESS COVER, ANTI-MICROBIAL is the device name listed in this FDA 510(k) record. The listed applicant is American Threshold Industries, Inc.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K832483. 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 MATTRESS COVER, ANTI-MICROBIAL?

MATTRESS COVER, ANTI-MICROBIAL is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is American Threshold Industries, Inc.. The 510(k) number is K832483.

When did MATTRESS COVER, ANTI-MICROBIAL receive FDA 510(k) clearance?

MATTRESS COVER, ANTI-MICROBIAL received FDA 510(k) clearance on 1984-02-04, under 510(k) number K832483.

Who is the listed applicant for MATTRESS COVER, ANTI-MICROBIAL?

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

What is the FDA product code for MATTRESS COVER, ANTI-MICROBIAL?

The FDA product code for MATTRESS COVER, ANTI-MICROBIAL is FMW.

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Other records listing American Threshold Industries, 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.

K971483SECURE-WRAP (TM) STERILIZATION WRAPK953879SURGEON'S CAPK953878BOUFFANT CAPK952115BARRIER GOWN, KOOL-GARD BACKLESS GOWNK952114KOOL GARD SINGLES GOWNK952116COVER GOWN

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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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