510(k) K811400

HEMAQUIK by Accra Laboratories, Inc. — Product Code IAF

K811400 is an FDA 510(k) premarket notification submitted by Accra Laboratories, Inc. for the device "HEMAQUIK". The FDA issued a decision of Substantially Equivalent on June 18, 1981. The device falls under product code IAF (Wright'S Stain), a Class I device regulated under 21 CFR 864.1850. Accra Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 18, 1981
Date Received
May 18, 1981
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