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)

VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR

K-Number: K051056 · 2005-10-20

ApplicantAlbert Browne , Ltd.
Decision Date2005-10-20
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR 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 2005-10-20 under 510(k) number K051056. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR?

VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR is a medical device that received FDA 510(k) clearance on 2005-10-20. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K051056.

When did VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR receive FDA 510(k) clearance?

VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR received FDA 510(k) clearance on 2005-10-20, under 510(k) number K051056.

Who is the listed applicant for VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR?

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 VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR?

The FDA product code for VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR is FRC.

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: FRC)

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.

K260766Celerity 5 HP Biological Indicator (LCB052)STERIS CorporationK252680Celerity™ 20 HP Biological IndicatorSTERIS CorporationK251122Terragene® Bionova® BT20 Biological IndicatorTerrageneK251452Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)SterisK250044Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)STERIS CorporationK250061Celerity IncubatorSTERIS 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.

↑