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)

SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS

K-Number: K915814 · 1992-03-27

ApplicantSirchie Finger Print Laboratories, Inc.
Decision Date1992-03-27
Product CodeJKA
Advisory CommitteeCH
DecisionUnknown

Device Summary

SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS is the device name listed in this FDA 510(k) record. The listed applicant is Sirchie Finger Print Laboratories, Inc.. It received FDA 510(k) clearance on 1992-03-27 under 510(k) number K915814. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS?

SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS is a medical device that received FDA 510(k) clearance on 1992-03-27. The listed applicant is Sirchie Finger Print Laboratories, Inc.. The 510(k) number is K915814.

When did SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS receive FDA 510(k) clearance?

SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS received FDA 510(k) clearance on 1992-03-27, under 510(k) number K915814.

Who is the listed applicant for SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS?

The FDA 510(k) record lists Sirchie Finger Print Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS?

The FDA product code for SEX CRIMES/SEX ASSAULT VICT/SUSPECT EVID COLL KITS is JKA.

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

Related Devices (Code: JKA)

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.

K262215Profoject™ Safety Sliding Blood Collection SetCMT Health PTE., Ltd.K252899Female Culture Device; Male Culture Device; Transfer Device; Access DeviceZhejiang Kindly Medical Device Co., Ltd.K260128BD Preset™ and BD A-Line™ Arterial Blood Collection SyringesBecton, Dickinson and CompanyK252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderBecton, Dickinson and CompanyK252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeBecton, Dickinson and CompanyK252040BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection TubesBecton, Dickinson and Company

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.

↑