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)

RAVEN BACTERIAL SPORE STRIPS

K-Number: K020026 · 2002-01-30

ApplicantRaven Biological Laboratories, Inc.
Decision Date2002-01-30
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAVEN BACTERIAL SPORE STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Raven Biological Laboratories, Inc.. It received FDA 510(k) clearance on 2002-01-30 under 510(k) number K020026. 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 RAVEN BACTERIAL SPORE STRIPS?

RAVEN BACTERIAL SPORE STRIPS is a medical device that received FDA 510(k) clearance on 2002-01-30. The listed applicant is Raven Biological Laboratories, Inc.. The 510(k) number is K020026.

When did RAVEN BACTERIAL SPORE STRIPS receive FDA 510(k) clearance?

RAVEN BACTERIAL SPORE STRIPS received FDA 510(k) clearance on 2002-01-30, under 510(k) number K020026.

Who is the listed applicant for RAVEN BACTERIAL SPORE STRIPS?

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

What is the FDA product code for RAVEN BACTERIAL SPORE STRIPS?

The FDA product code for RAVEN BACTERIAL SPORE STRIPS 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 Raven Biological 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.

K082756RAVEN PROTEST - STEAM BIOLOGICAL INDICATORK062651PROCHEM EXT CHEMICAL INTEGRATORK053212RAVEN PROPACTK050591MODIFICATION TO RAVEN BACTERIAL SPORE STRIPSK041784RAVEN PROTEST - EOK041386RAVEN PROTEST - STEAM

View all 15 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.

↑