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FDA 510(k)

WIPEABLE PILLOW

K-Number: K924477 · 1993-01-29

ApplicantPerfect Fit Industries, Inc.
Decision Date1993-01-29
Product CodeFMW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WIPEABLE PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Perfect Fit Industries, Inc.. It received FDA 510(k) clearance on 1993-01-29 under 510(k) number K924477. 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 WIPEABLE PILLOW?

WIPEABLE PILLOW is a medical device that received FDA 510(k) clearance on 1993-01-29. The listed applicant is Perfect Fit Industries, Inc.. The 510(k) number is K924477.

When did WIPEABLE PILLOW receive FDA 510(k) clearance?

WIPEABLE PILLOW received FDA 510(k) clearance on 1993-01-29, under 510(k) number K924477.

Who is the listed applicant for WIPEABLE PILLOW?

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

What is the FDA product code for WIPEABLE PILLOW?

The FDA product code for WIPEABLE PILLOW is FMW.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Perfect Fit 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.

K924807REUSABLE INCONTIENT UNDERPAD

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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