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)

BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER

K-Number: K961832 · 1996-09-06

ApplicantBlue Ridge Medical, Inc.
Decision Date1996-09-06
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER is the device name listed in this FDA 510(k) record. The listed applicant is Blue Ridge Medical, Inc.. It received FDA 510(k) clearance on 1996-09-06 under 510(k) number K961832. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER?

BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER is a medical device that received FDA 510(k) clearance on 1996-09-06. The listed applicant is Blue Ridge Medical, Inc.. The 510(k) number is K961832.

When did BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER receive FDA 510(k) clearance?

BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER received FDA 510(k) clearance on 1996-09-06, under 510(k) number K961832.

Who is the listed applicant for BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER?

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

What is the FDA product code for BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER?

The FDA product code for BLUE RIDGE PRODUCTS LARYNGOSCOPE BLADE COVER is CCW.

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

Related Devices (Code: CCW)

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.

K191602APA Oxy BladeVenner Medical (Singapore) Pte, Ltd.K163412Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL)Girgis Scope, LLCK121378AIRTRAQ SP AIRTRAQ AVANTProdol Meditec , Ltd.K063477NOVAMED MRI CONDITIONAL LARYNGOSCOPE SETNovamed, LLCK062523TRU-MR LARYNGOSCOPE SETTruphatek International, Ltd.K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002Minrad, Inc.

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.

↑