KODAK EKTACHEM CLINICAL CHEM. NH3

Photometric Method, Ammonia

EASTMAN KODAK COMPANY

The following data is part of a premarket notification filed by Eastman Kodak Company with the FDA for Kodak Ektachem Clinical Chem. Nh3.

Pre-market Notification Details

• Device ID: K820723
• 510k Number: K820723
• Device Name: KODAK EKTACHEM CLINICAL CHEM. NH3
• Classification: Photometric Method, Ammonia
• Applicant: EASTMAN KODAK COMPANY 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: JID
• CFR Regulation Number: 862.1065 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1982-03-16
• Decision Date: 1982-04-01

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10758750009602	K820723	000
10758750000012	K820723	000