NOSECLIP #6118— 510(k) K810339

Name: FDA 510(k) clearance K810339
Creator: U.S. Food and Drug Administration
Published: 1981-03-17

Substantially Equivalent

Todd Industries, Inc.

FDA 510(k) clearance K810339 for NOSECLIP #6118, Substantially Equivalent on 1981-03-17. Applicant: Todd Industries, Inc.. Device class: 1.

Clearance details

Applicant: Todd Industries, Inc.
Product code: Code BXJ
Device class: Class 1
Regulation: 21 CFR 868.6225
Advisory panel: Anesthesiology
Date received: 1981-02-09
Decision date: 1981-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXJ

view all

K853578 — MEDIPART DISPOS. NOSE CLIP MP-20011985-10-29
K770015 — NOSECLIP FOR RESP. CARE & PULMON. FUNC.1977-03-16
K760461 — NOSE CLIP1976-08-26

More clearances from Todd Industries, Inc.

view all

K810340 — ADULT MASKS & PEDIATRIC MASKS1981-03-17
K810341 — LIFELINE IPPB SET-UP1981-03-17
K810342 — NASAL CANNULA1981-03-17
K810343 — NEBULIZERS1981-03-17
K810344 — OXYGEN TUBING1981-03-17

Adverse events under product code BXJ

product code BXJ

Other: 1
Total: 1

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.