DeviceClearance

KODAK AMERLITE CK-MB CONTROL SERA LAN.4413— 510(k) K925880

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K925880 for KODAK AMERLITE CK-MB CONTROL SERA LAN.4413, Substantially Equivalent on 1993-02-05. Applicant: Eastman Kodak Company.

Clearance details

Applicant
Eastman Kodak Company
Product code
Code JJX
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Rochester, NY, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code JJX

product code JJX
Other
2
Total
2

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.