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)

DAMON D.E.T.E.C.T IMAGE ENHANCER

K-Number: K874865 · 1987-12-23

ApplicantDamon Corp.
Decision Date1987-12-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DAMON D.E.T.E.C.T IMAGE ENHANCER is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1987-12-23 under 510(k) number K874865. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAMON D.E.T.E.C.T IMAGE ENHANCER?

DAMON D.E.T.E.C.T IMAGE ENHANCER is a medical device that received FDA 510(k) clearance on 1987-12-23. The listed applicant is Damon Corp.. The 510(k) number is K874865.

When did DAMON D.E.T.E.C.T IMAGE ENHANCER receive FDA 510(k) clearance?

DAMON D.E.T.E.C.T IMAGE ENHANCER received FDA 510(k) clearance on 1987-12-23, under 510(k) number K874865.

Who is the listed applicant for DAMON D.E.T.E.C.T IMAGE ENHANCER?

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

What is the FDA product code for DAMON D.E.T.E.C.T IMAGE ENHANCER?

The FDA product code for DAMON D.E.T.E.C.T IMAGE ENHANCER is LLZ.

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 Damon 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.

K831826ADRENOCORTICOTROPIN RADIO-IMMUNOASSAYK820686LIQUISOL PROGESTERONE RADIOIMMUNOK802661LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK790250LIQUISOL CORTISOL RIA TEST KITK782124IEC CENTRA-7 CENTRIFUGE MODEL 2362K781012RIA TEST KIT SYS. DAMON KIQUISOL FREE

View all 11 devices →

Related Devices (Code: LLZ)

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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.

↑