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FDA 510(k)

DISINFECTION WITH THE COX DRY HEAT STERILIZER

K-Number: K910925 · 1992-05-08

Decision Date1992-05-08
Product CodeKMH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISINFECTION WITH THE COX DRY HEAT STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Cox Sterile Products, Inc.. It received FDA 510(k) clearance on 1992-05-08 under 510(k) number K910925. The device is classified under product code KMH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISINFECTION WITH THE COX DRY HEAT STERILIZER?

DISINFECTION WITH THE COX DRY HEAT STERILIZER is a medical device that received FDA 510(k) clearance on 1992-05-08. The listed applicant is Cox Sterile Products, Inc.. The 510(k) number is K910925.

When did DISINFECTION WITH THE COX DRY HEAT STERILIZER receive FDA 510(k) clearance?

DISINFECTION WITH THE COX DRY HEAT STERILIZER received FDA 510(k) clearance on 1992-05-08, under 510(k) number K910925.

Who is the listed applicant for DISINFECTION WITH THE COX DRY HEAT STERILIZER?

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

What is the FDA product code for DISINFECTION WITH THE COX DRY HEAT STERILIZER?

The FDA product code for DISINFECTION WITH THE COX DRY HEAT STERILIZER is KMH.

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.

Other records listing Cox Sterile Products, 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.

Related Devices (Code: KMH)

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.

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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