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FDA 510(k)

THORACIC SUPPORT SYSTEM

K-Number: K883214 · 1989-01-17

ApplicantStorer Medical Products
Decision Date1989-01-17
Product CodeKMO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THORACIC SUPPORT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Storer Medical Products. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K883214. 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 THORACIC SUPPORT SYSTEM?

THORACIC SUPPORT SYSTEM is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Storer Medical Products. The 510(k) number is K883214.

When did THORACIC SUPPORT SYSTEM receive FDA 510(k) clearance?

THORACIC SUPPORT SYSTEM received FDA 510(k) clearance on 1989-01-17, under 510(k) number K883214.

Who is the listed applicant for THORACIC SUPPORT SYSTEM?

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

What is the FDA product code for THORACIC SUPPORT SYSTEM?

The FDA product code for THORACIC SUPPORT SYSTEM 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.K893809COUGH PILLOWCustom Hospitals 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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