510(k) K902360

HEMA-SCREEN by Immunostics Co., Inc. — Product Code KHE

K902360 is an FDA 510(k) premarket notification submitted by Immunostics Co., Inc. for the device "HEMA-SCREEN". The FDA issued a decision of Substantially Equivalent on July 27, 1990. The device falls under product code KHE (Reagent, Occult Blood), a Class II device regulated under 21 CFR 864.6550. Immunostics Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 27, 1990
Date Received
May 29, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagent, Occult Blood
Device Class
Class II
Regulation Number
864.6550
Review Panel
HE
Submission Type