VIDEO SCOPE SYSTEM (NASOPHARYNGOSCOPE {FLEXIBLE OR RIGID})— 510(k) K944671

Name: FDA 510(k) clearance K944671
Creator: U.S. Food and Drug Administration
Published: 1995-02-07

Substantially Equivalent

Jedmed Instrument Co.

FDA 510(k) clearance K944671 for VIDEO SCOPE SYSTEM (NASOPHARYNGOSCOPE {FLEXIBLE OR RIGID}), Substantially Equivalent on 1995-02-07. Applicant: Jedmed Instrument Co.. Device class: 2.

Clearance details

Applicant: Jedmed Instrument Co.
Product code: Code EOB
Device class: Class 2
Regulation: 21 CFR 874.4760
Advisory panel: Ear, Nose, Throat
Date received: 1994-09-22
Decision date: 1995-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St.Louis, MO, US

Download summary PDF View on FDA.gov ↗

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K132039 — ERGO-FLEX LARYNGO-NASOPHARYNGOSCOPE EF-N AND EF-N SLIM2014-02-21
K021750 — LID CHAIN EYELID WEIGHTS2003-01-27
K954184 — JED-LIGHT FIBEROPTIC LIGHT SOURCE1995-11-13
K944032 — VIDEO SCOPE SYSTEM (LARYNGOSCOPE)1995-09-15
K950925 — JEDMED LARYNGEAL SCOPE1995-08-11

Adverse events under product code EOB

product code EOB

Malfunction: 6,143
Total: 6,143

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.