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)

LDC UVIII FIXED WAVELENGTH ULTRAVIOLET

K-Number: K800047 · 1980-01-21

ApplicantLaboratory Data Control
Decision Date1980-01-21
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LDC UVIII FIXED WAVELENGTH ULTRAVIOLET is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory Data Control. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K800047. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LDC UVIII FIXED WAVELENGTH ULTRAVIOLET?

LDC UVIII FIXED WAVELENGTH ULTRAVIOLET is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Laboratory Data Control. The 510(k) number is K800047.

When did LDC UVIII FIXED WAVELENGTH ULTRAVIOLET receive FDA 510(k) clearance?

LDC UVIII FIXED WAVELENGTH ULTRAVIOLET received FDA 510(k) clearance on 1980-01-21, under 510(k) number K800047.

Who is the listed applicant for LDC UVIII FIXED WAVELENGTH ULTRAVIOLET?

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

What is the FDA product code for LDC UVIII FIXED WAVELENGTH ULTRAVIOLET?

The FDA product code for LDC UVIII FIXED WAVELENGTH ULTRAVIOLET is KIE.

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 Laboratory Data Control 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.

K800289LDC SPECTROMONITOR IIIK800046LDC CHROMATOGRAPHY ACCESSORY MODULE BK800048LDC CONSTAMETRIC III HIGHT PRESS. SOL.

Related Devices (Code: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore 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.

↑