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FDA 510(k)

U. V. GERMICIDAL UNIT

K-Number: K871615 · 1987-09-11

ApplicantLorvic Corp.
Decision Date1987-09-11
Product CodeKMH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

U. V. GERMICIDAL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Lorvic Corp.. It received FDA 510(k) clearance on 1987-09-11 under 510(k) number K871615. 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 U. V. GERMICIDAL UNIT?

U. V. GERMICIDAL UNIT is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is Lorvic Corp.. The 510(k) number is K871615.

When did U. V. GERMICIDAL UNIT receive FDA 510(k) clearance?

U. V. GERMICIDAL UNIT received FDA 510(k) clearance on 1987-09-11, under 510(k) number K871615.

Who is the listed applicant for U. V. GERMICIDAL UNIT?

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

What is the FDA product code for U. V. GERMICIDAL UNIT?

The FDA product code for U. V. GERMICIDAL UNIT 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 Lorvic Corp. 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.

K780263SHIELDK770063DISP. ABSORBENT COMPRESSED FIBRE WAFERK770064FLUORIDE GEL DISPOSABLE TRAYK760620SALIVA EJECTORK760121IMPULSE HEAT SEALER

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

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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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