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FDA 510(k)

COUGH PILLOW

K-Number: K893809 · 1989-08-28

ApplicantCustom Hospitals Products
Decision Date1989-08-28
Product CodeKMO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COUGH PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Custom Hospitals Products. It received FDA 510(k) clearance on 1989-08-28 under 510(k) number K893809. The device is classified under product code KMO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COUGH PILLOW?

COUGH PILLOW is a medical device that received FDA 510(k) clearance on 1989-08-28. The listed applicant is Custom Hospitals Products. The 510(k) number is K893809.

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

COUGH PILLOW received FDA 510(k) clearance on 1989-08-28, under 510(k) number K893809.

Who is the listed applicant for COUGH PILLOW?

The FDA 510(k) record lists Custom Hospitals Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COUGH PILLOW?

The FDA product code for COUGH PILLOW is KMO.

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Related Devices (Code: KMO)

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.

K9218524 SURE TM RECTAL TUBEBoston Pacific Medical, Inc.K883214THORACIC SUPPORT SYSTEMStorer Medical ProductsK882592HEART HUGGER STERNUM SUPPORT HARNESSGeneral Cardiac Technology, Inc.K792629STERILIZATION PROCESS/T-BINDERProcter & Gamble Mfg. Co.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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