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)

SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF

K-Number: K052485 · 2006-01-17

ApplicantMidi, Inc.
Decision Date2006-01-17
Product CodeNWZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF is the device name listed in this FDA 510(k) record. The listed applicant is Midi, Inc.. It received FDA 510(k) clearance on 2006-01-17 under 510(k) number K052485. The device is classified under product code NWZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF?

SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF is a medical device that received FDA 510(k) clearance on 2006-01-17. The listed applicant is Midi, Inc.. The 510(k) number is K052485.

When did SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF receive FDA 510(k) clearance?

SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF received FDA 510(k) clearance on 2006-01-17, under 510(k) number K052485.

Who is the listed applicant for SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF?

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

What is the FDA product code for SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF?

The FDA product code for SHERLOCK MICROBIAL IDENTIFICATION SYSTEM FOR BIODEF is NWZ.

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 Midi, 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.

K020689SHERLOCK MYCOBACTERIA IDENTIFICATION SYSTEM

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.

↑