LARYNGOSCOPE— 510(k) K883296

Name: FDA 510(k) clearance K883296
Creator: U.S. Food and Drug Administration
Published: 1988-10-13

Substantially Equivalent

Lothar Scharras

FDA 510(k) clearance K883296 for LARYNGOSCOPE, Substantially Equivalent on 1988-10-13. Applicant: Lothar Scharras. Device class: 1.

Clearance details

Applicant: Lothar Scharras
Product code: Code CCW
Device class: Class 1
Regulation: 21 CFR 868.5540
Advisory panel: Anesthesiology
Date received: 1988-08-04
Decision date: 1988-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CCW

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K191602 — APA Oxy Blade2019-08-02
K163412 — Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL)2017-06-22
K140951 — YEESCOPE LARYNGOSCOPES2014-11-10
K121378 — AIRTRAQ SP AIRTRAQ AVANT2012-06-21
K063477 — NOVAMED MRI CONDITIONAL LARYNGOSCOPE SET2007-02-09

Adverse events under product code CCW

product code CCW

Death: 31
Injury: 136
Malfunction: 3,703
Other: 1
Total: 3,871

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.