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FDA 510(k)

DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST

K-Number: K902446 · 1990-08-10

ApplicantMallinckrodt Group, Inc.
Decision Date1990-08-10
Product CodeFMW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1990-08-10 under 510(k) number K902446. 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 DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST?

DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST is a medical device that received FDA 510(k) clearance on 1990-08-10. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K902446.

When did DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST receive FDA 510(k) clearance?

DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST received FDA 510(k) clearance on 1990-08-10, under 510(k) number K902446.

Who is the listed applicant for DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST?

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

What is the FDA product code for DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST?

The FDA product code for DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST is FMW.

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Other records listing Mallinckrodt Group, 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.

K945053LF CT HIG PRESSURE CATHETERSK945140URO-FLOK943581HYDRADJUST IV UROLOGICAL TABLEK943122SURGICAL DRAPESK934664HYDRAGOWNK920742HYDRAJUST IV UROLOGICAL TABLE

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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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