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)

BROWNE GA INDICATOR FOR CIDEX PRODUCTS

K-Number: K981054 · 1998-12-07

ApplicantAlbert Browne , Ltd.
Decision Date1998-12-07
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE GA INDICATOR FOR CIDEX PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Albert Browne , Ltd.. It received FDA 510(k) clearance on 1998-12-07 under 510(k) number K981054. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BROWNE GA INDICATOR FOR CIDEX PRODUCTS?

BROWNE GA INDICATOR FOR CIDEX PRODUCTS is a medical device that received FDA 510(k) clearance on 1998-12-07. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K981054.

When did BROWNE GA INDICATOR FOR CIDEX PRODUCTS receive FDA 510(k) clearance?

BROWNE GA INDICATOR FOR CIDEX PRODUCTS received FDA 510(k) clearance on 1998-12-07, under 510(k) number K981054.

Who is the listed applicant for BROWNE GA INDICATOR FOR CIDEX PRODUCTS?

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

What is the FDA product code for BROWNE GA INDICATOR FOR CIDEX PRODUCTS?

The FDA product code for BROWNE GA INDICATOR FOR CIDEX PRODUCTS is JOJ.

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 Albert Browne , Ltd. 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.

K063285RELIANCE CI PROCESS INDICATORK061738ALBERT BROWNE LTD. VERIFY STEAM AND EO LOAD RECORD CARDK053479VERIFY DRY HEAT LABELK060066VERIFY 3-10 MIN FLASH INTEGRATORK060103ALBERT BROWNE LTD. VERIFY STEAM VALUE INDICATORSK051101VERIFY FLASH INTEGRATOR

View all 19 devices →

Related Devices (Code: JOJ)

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.

K2619923M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)Solventum US, LLCK260181LF Process Indicator Tape for Steam SterilizationIntertape Polymer GroupK251991SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213)Shenzhen Safesecure Medical Infection Control Tech Co. , Ltd.K251035DISINTEK™ PA Test StripsSerim ResearchK251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118STERIS CorporationK243876VERIFY STEAM Integrating IndicatorSTERIS Corporation

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.

↑