VAPORIZER, ANESTHESIA, NON-HEATED— 510(k) K882500

Name: FDA 510(k) clearance K882500
Creator: U.S. Food and Drug Administration
Published: 1988-08-01

Substantially Equivalent

Anesthetic Vaporizer Services

FDA 510(k) clearance K882500 for VAPORIZER, ANESTHESIA, NON-HEATED, Substantially Equivalent on 1988-08-01. Applicant: Anesthetic Vaporizer Services. Device class: 2.

Clearance details

Applicant: Anesthetic Vaporizer Services
Product code: Code CAD
Device class: Class 2
Regulation: 21 CFR 868.5880
Advisory panel: Anesthesiology
Date received: 1988-06-17
Decision date: 1988-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAD

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K240375 — V80 Anesthetic Vaporizer (V80)2024-10-31
K172702 — Tec 820, Tec 8502018-01-04
K150167 — V60 Anesthetic Vaporizer2015-06-30
K110608 — SEVOFLURANE VAPORIZER ADAPTOR2011-07-20
K060331 — SIGMA ALPHA VAPORIZER2006-05-10

Adverse events under product code CAD

product code CAD

Malfunction: 3,275
Total: 3,275

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.