510(k) K790571

QUIK-STAIN by Dade, Baxter Travenol Diagnostics, Inc. — Product Code IAF

K790571 is an FDA 510(k) premarket notification submitted by Dade, Baxter Travenol Diagnostics, Inc. for the device "QUIK-STAIN". The FDA issued a decision of Substantially Equivalent on April 23, 1979. The device falls under product code IAF (Wright'S Stain), a Class I device regulated under 21 CFR 864.1850. Dade, Baxter Travenol Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 23, 1979
Date Received
March 23, 1979
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