BLOODBORNE PATHOGEN KIT— 510(k) K953102

Substantially Equivalent

Certified Safety Mfg., Inc.

FDA 510(k) clearance K953102 for BLOODBORNE PATHOGEN KIT, Substantially Equivalent on 1995-12-11. Applicant: Certified Safety Mfg., Inc.. Device class: 2.

Clearance details

Applicant
Certified Safety Mfg., Inc.
Product code
Code FXX
Device class
Class 2
Regulation
21 CFR 878.4040
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Kansas City, MO, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code FXX

product code FXX
Injury
137
Total
137

Source: openFDA MAUDE database, through . 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.