STERETS INJECTION SWAB— 510(k) K852235

Name: FDA 510(k) clearance K852235
Creator: U.S. Food and Drug Administration
Published: 1985-06-07

Substantially Equivalent

Ellis Pharmaceutical Consulting, Inc.

FDA 510(k) clearance K852235 for STERETS INJECTION SWAB, Substantially Equivalent on 1985-06-07. Applicant: Ellis Pharmaceutical Consulting, Inc.. Device class: Unclassified.

Clearance details

Applicant: Ellis Pharmaceutical Consulting, Inc.
Product code: Code LKB
Device class: Unclassified
Advisory panel: Unknown
Date received: 1985-05-22
Decision date: 1985-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LKB

product code LKB

Other: 2
Total: 2

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.