510(k) K834595

PARAGON ACID HEMOGLOBIN REAGENT KIT by Beckman Instruments, Inc. — Product Code GKA

K834595 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "PARAGON ACID HEMOGLOBIN REAGENT KIT". The FDA issued a decision of Substantially Equivalent on May 7, 1984. The device falls under product code GKA (Abnormal Hemoglobin Quantitation), a Class II device regulated under 21 CFR 864.7415. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 1984
Date Received
December 30, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Abnormal Hemoglobin Quantitation
Device Class
Class II
Regulation Number
864.7415
Review Panel
HE
Submission Type