510(k) K890673

WRIGHT-GLEMSA STAIN by Sigma Diagnostics, Inc. — Product Code IAF

K890673 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "WRIGHT-GLEMSA STAIN". The FDA issued a decision of Substantially Equivalent on February 24, 1989. The device falls under product code IAF (Wright'S Stain), a Class I device regulated under 21 CFR 864.1850. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1989
Date Received
February 9, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wright'S Stain
Device Class
Class I
Regulation Number
864.1850
Review Panel
PA
Submission Type