510(k) K853241

HEMATOLOGY STAIN PACK by Fisher Scientific Co., LLC — Product Code IAF

K853241 is an FDA 510(k) premarket notification submitted by Fisher Scientific Co., LLC for the device "HEMATOLOGY STAIN PACK". The FDA issued a decision of Substantially Equivalent on August 19, 1985. The device falls under product code IAF (Wright'S Stain), a Class I device regulated under 21 CFR 864.1850. Fisher Scientific Co., LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 19, 1985
Date Received
August 1, 1985
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