CARBON MEDICAL TECHNOLOGIES INJECTION NEEDLE— 510(k) K030451

Substantially Equivalent

Carbon Medical Technologies, Inc.

FDA 510(k) clearance K030451 for CARBON MEDICAL TECHNOLOGIES INJECTION NEEDLE, Substantially Equivalent on 2003-04-30. Applicant: Carbon Medical Technologies, Inc..

Clearance details

Applicant: Carbon Medical Technologies, Inc.
Product code: Code FBK
Advisory panel: Gastroenterology, Urology
Date received: 2003-02-11
Decision date: 2003-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FBK

product code FBK

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.