510(k) K897147

SIGMA PROCEDURE NO. 735 by Sigma Diagnostics, Inc. — Product Code KHP

K897147 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "SIGMA PROCEDURE NO. 735". The FDA issued a decision of Substantially Equivalent on April 3, 1990. The device falls under product code KHP (Acid, Lactic, Enzymatic Method), a Class I device regulated under 21 CFR 862.1450. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 3, 1990
Date Received
December 26, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Lactic, Enzymatic Method
Device Class
Class I
Regulation Number
862.1450
Review Panel
CH
Submission Type