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)

LARYNGOSCOPE

K-Number: K883296 · 1988-10-13

ApplicantLothar Scharras
Decision Date1988-10-13
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Lothar Scharras. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K883296. 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 LARYNGOSCOPE?

LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Lothar Scharras. The 510(k) number is K883296.

When did LARYNGOSCOPE receive FDA 510(k) clearance?

LARYNGOSCOPE received FDA 510(k) clearance on 1988-10-13, under 510(k) number K883296.

Who is the listed applicant for LARYNGOSCOPE?

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

What is the FDA product code for LARYNGOSCOPE?

The FDA product code for LARYNGOSCOPE 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.

↑