LANCER COAGENT APTT KIT

Test, Time, Partial Thromboplastin

SHERWOOD MEDICAL CO.

The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Lancer Coagent Aptt Kit.

Pre-market Notification Details

• Device ID: K792048
• 510k Number: K792048
• Device Name: LANCER COAGENT APTT KIT
• Classification: Test, Time, Partial Thromboplastin
• Applicant: SHERWOOD MEDICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: GGW
• CFR Regulation Number: 864.7925 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-10-12
• Decision Date: 1979-11-05

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
03607450005974	K792048	000