Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIC 180 MEDICAL LAMPS

K-Number: K812142 · 1981-08-13

ApplicantLada Intl., Inc.
Decision Date1981-08-13
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIC 180 MEDICAL LAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Lada Intl., Inc.. It received FDA 510(k) clearance on 1981-08-13 under 510(k) number K812142. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIC 180 MEDICAL LAMPS?

LIC 180 MEDICAL LAMPS is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Lada Intl., Inc.. The 510(k) number is K812142.

When did LIC 180 MEDICAL LAMPS receive FDA 510(k) clearance?

LIC 180 MEDICAL LAMPS received FDA 510(k) clearance on 1981-08-13, under 510(k) number K812142.

Who is the listed applicant for LIC 180 MEDICAL LAMPS?

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

What is the FDA product code for LIC 180 MEDICAL LAMPS?

The FDA product code for LIC 180 MEDICAL LAMPS is KZF.

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 Lada Intl., 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.

K872833BREATHGUARD APNEA MONITORK861410LIC MOBILE TRANSPORT STRETCHERSK830050MOLNLYCKE MEPORE STERILE SELF-ADHESIVEK830166MOLNLYCKE ETE STERILE NON-ADHERENT DRESSK830051MOLNLYCKE MESALT STERILE DRESSINGK812141LIC OBSTETRICAL TABLE

View all 7 devices →

Related Devices (Code: KZF)

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.

K954943NEVOSCOPENizar A. MullaniK952835WELCH ALLYN VIDEO EPISCOPEWelch Allyn, Inc.K945507H 5100, H 5200, H 5300Rudolf Riester GmbH & Co. KGK941869SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEGThe Lighthouse For the Blind, Inc.K936088WAVE FLUORESCENT MAGNIFIERBurton Medical Products Corp.K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONMeddev International Corp.

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.

↑