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)

TITERTEK-ENTEROBAC RAPID AUTOMATED

K-Number: K842182 · 1984-06-01

ApplicantFlow Laboratories, Inc.
Decision Date1984-06-01
Product Code
DecisionUnknown

Device Summary

TITERTEK-ENTEROBAC RAPID AUTOMATED is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K842182. FDA Decision: Unknown.

Frequently Asked Questions

What is the TITERTEK-ENTEROBAC RAPID AUTOMATED?

TITERTEK-ENTEROBAC RAPID AUTOMATED is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K842182.

When did TITERTEK-ENTEROBAC RAPID AUTOMATED receive FDA 510(k) clearance?

TITERTEK-ENTEROBAC RAPID AUTOMATED received FDA 510(k) clearance on 1984-06-01, under 510(k) number K842182.

Who is the listed applicant for TITERTEK-ENTEROBAC RAPID AUTOMATED?

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

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 Flow Laboratories, 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.

K861897UNISKAN IIK862066TITERTEK MICROPLATE WASHER S-12K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEK861823GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)K861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)K860762GAMMA-FREE HORSE SERUM

View all 57 devices →

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.

↑