NOSE CLIP— 510(k) K760461

Name: FDA 510(k) clearance K760461
Creator: U.S. Food and Drug Administration
Published: 1976-08-26

Substantially Equivalent

Inspiron Corp.

FDA 510(k) clearance K760461 for NOSE CLIP, Substantially Equivalent on 1976-08-26. Applicant: Inspiron Corp.. Device class: 1.

Clearance details

Applicant: Inspiron Corp.
Product code: Code BXJ
Device class: Class 1
Regulation: 21 CFR 868.6225
Advisory panel: Anesthesiology
Date received: 1976-08-18
Decision date: 1976-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K853578 — MEDIPART DISPOS. NOSE CLIP MP-20011985-10-29
K810339 — NOSECLIP #61181981-03-17
K770015 — NOSECLIP FOR RESP. CARE & PULMON. FUNC.1977-03-16

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K840935 — MANUAL RESUSCITATION SYSTEM1984-04-05
K841158 — NEBULO 28 NEBULIZER KIT1984-03-30

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.