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)

BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P

K-Number: K883819 · 1988-10-17

ApplicantCircon Acmi
Decision Date1988-10-17
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P is the device name listed in this FDA 510(k) record. The listed applicant is Circon Acmi. It received FDA 510(k) clearance on 1988-10-17 under 510(k) number K883819. 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 BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P?

BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P is a medical device that received FDA 510(k) clearance on 1988-10-17. The listed applicant is Circon Acmi. The 510(k) number is K883819.

When did BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P receive FDA 510(k) clearance?

BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P received FDA 510(k) clearance on 1988-10-17, under 510(k) number K883819.

Who is the listed applicant for BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P?

The FDA 510(k) record lists Circon Acmi as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P?

The FDA product code for BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P 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

Other records listing Circon Acmi 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.

K013165USA SERIES LAPAROSCOPESK980492AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)K905706GYN-1500 HYSTEROSCOPIC INUFFLATORK905705LAP 3501 HIGH FLOW INSUFFLATORK884097MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPESK884025CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200

View all 10 devices →

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.

↑