SPECTRO FEIRITIN

Ferritin, Antigen, Antiserum, Control

RAMCO LABORATORIES, INC.

The following data is part of a premarket notification filed by Ramco Laboratories, Inc. with the FDA for Spectro Feiritin.

Pre-market Notification Details

• Device ID: K812056
• 510k Number: K812056
• Device Name: SPECTRO FEIRITIN
• Classification: Ferritin, Antigen, Antiserum, Control
• Applicant: RAMCO LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: DBF
• CFR Regulation Number: 866.5340 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1981-07-21
• Decision Date: 1981-08-12

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
08600000686017	K812056	000