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)

TRENDS LANCET

K-Number: K843882 · 1984-11-05

ApplicantOrange Medical Instruments, Inc.
Decision Date1984-11-05
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRENDS LANCET is the device name listed in this FDA 510(k) record. The listed applicant is Orange Medical Instruments, Inc.. It received FDA 510(k) clearance on 1984-11-05 under 510(k) number K843882. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRENDS LANCET?

TRENDS LANCET is a medical device that received FDA 510(k) clearance on 1984-11-05. The listed applicant is Orange Medical Instruments, Inc.. The 510(k) number is K843882.

When did TRENDS LANCET receive FDA 510(k) clearance?

TRENDS LANCET received FDA 510(k) clearance on 1984-11-05, under 510(k) number K843882.

Who is the listed applicant for TRENDS LANCET?

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

What is the FDA product code for TRENDS LANCET?

The FDA product code for TRENDS LANCET is KMK.

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 Orange Medical Instruments, 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.

K860808CONTINUCATHK851822BETA SCAN TRENDS METERK844796MICRO-BETA U100 SYRINGEK841369BETA SCAN DRYSTIXK833705BETAJECT BD U100K833706CLICK-COUNT U100 INSULIN SYRINGE

View all 12 devices →

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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.

↑