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FDA 510(k)

COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE

K-Number: K881371 · 1988-04-13

ApplicantCox Sterile Products, Inc.
Decision Date1988-04-13
Product CodeKMH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE 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 1988-04-13 under 510(k) number K881371. 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 COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE?

COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE is a medical device that received FDA 510(k) clearance on 1988-04-13. The listed applicant is Cox Sterile Products, Inc.. The 510(k) number is K881371.

When did COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE receive FDA 510(k) clearance?

COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE received FDA 510(k) clearance on 1988-04-13, under 510(k) number K881371.

Who is the listed applicant for COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE?

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 COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE?

The FDA product code for COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE 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.

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 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.

K922440STERIKING, SEE & PEELK910925DISINFECTION WITH THE COX DRY HEAT STERILIZERK872643COX RAPID HEAT TRANSFER STERILIZER

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.

K094026STERI-DENT, STERI-SURECpac, Inc.K051660DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEMColtene/Whaledent, Inc.K910925DISINFECTION WITH THE COX DRY HEAT STERILIZERCox Sterile Products, Inc.K910202DENTRONIX MODEL 2000Dentronix, Inc.K880322DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEMDentronix, Inc.K872643COX RAPID HEAT TRANSFER STERILIZERCox Sterile Products, Inc.

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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