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FDA 510(k)

HOME CARE WATER FLOTATION BED HC4/TC/H

K-Number: K840882 · 1984-07-18

ApplicantWestern Medical, Ltd.
Decision Date1984-07-18
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HOME CARE WATER FLOTATION BED HC4/TC/H is the device name listed in this FDA 510(k) record. The listed applicant is Western Medical, Ltd.. It received FDA 510(k) clearance on 1984-07-18 under 510(k) number K840882. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOME CARE WATER FLOTATION BED HC4/TC/H?

HOME CARE WATER FLOTATION BED HC4/TC/H is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Western Medical, Ltd.. The 510(k) number is K840882.

When did HOME CARE WATER FLOTATION BED HC4/TC/H receive FDA 510(k) clearance?

HOME CARE WATER FLOTATION BED HC4/TC/H received FDA 510(k) clearance on 1984-07-18, under 510(k) number K840882.

Who is the listed applicant for HOME CARE WATER FLOTATION BED HC4/TC/H?

The FDA 510(k) record lists Western Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOME CARE WATER FLOTATION BED HC4/TC/H?

The FDA product code for HOME CARE WATER FLOTATION BED HC4/TC/H is IOQ.

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.

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Other records listing Western Medical, Ltd. 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.

K894387WESTCO MADAYAG PAB NEEDLEK891459STERILE BURNNET PRE-CUT (VARIOUS SIZES)K840881WATER FLOATION BED 800/TC/H

Related Devices (Code: IOQ)

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.

K122473TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2Hill-RomK973624NURSE'S AID PATIENT ROTATION SYSTEMAir Med Assist ProductsK970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, 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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