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FDA 510(k)

DRY HEAT STERILIZER

K-Number: K771070 · 1977-07-14

ApplicantCpac, Inc.
Decision Date1977-07-14
Product CodeKMH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DRY HEAT STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Cpac, Inc.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771070. 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 DRY HEAT STERILIZER?

DRY HEAT STERILIZER is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Cpac, Inc.. The 510(k) number is K771070.

When did DRY HEAT STERILIZER receive FDA 510(k) clearance?

DRY HEAT STERILIZER received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771070.

Who is the listed applicant for DRY HEAT STERILIZER?

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

What is the FDA product code for DRY HEAT STERILIZER?

The FDA product code for 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.

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 Cpac, 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.

K110867STERI-DENT, STERI-SUREK094026STERI-DENT, STERI-SUREK781486STERI-VAC POWER UNITSK771071PORTO-VAC

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.K881371COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLECox Sterile Products, 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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