ASTRA DISPOSABLE SPRAY CANNULA— 510(k) K894755

Name: FDA 510(k) clearance K894755
Creator: U.S. Food and Drug Administration
Published: 1990-01-12

Substantially Equivalent

Astra Pharmaceutical Products, Inc.

FDA 510(k) clearance K894755 for ASTRA DISPOSABLE SPRAY CANNULA, Substantially Equivalent on 1990-01-12. Applicant: Astra Pharmaceutical Products, Inc.. Device class: 2.

Clearance details

Applicant: Astra Pharmaceutical Products, Inc.
Product code: Code CCT
Device class: Class 2
Regulation: 21 CFR 868.5170
Advisory panel: Anesthesiology
Date received: 1989-07-27
Decision date: 1990-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westborough, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CCT

product code CCT

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.