NOSECLIP FOR RESP. CARE & PULMON. FUNC.— 510(k) K770015

Name: FDA 510(k) clearance K770015
Creator: U.S. Food and Drug Administration
Published: 1977-03-16

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K770015 for NOSECLIP FOR RESP. CARE & PULMON. FUNC., Substantially Equivalent on 1977-03-16. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code BXJ
Device class: Class 1
Regulation: 21 CFR 868.6225
Advisory panel: Anesthesiology
Date received: 1977-01-03
Decision date: 1977-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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
K760461 — NOSE CLIP1976-08-26

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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.