510(k) K952437

DMA GLUCOSE HEXOKINASE U.V. PROCEDURE by Data Medical Associates, Inc. — Product Code CFR

K952437 is an FDA 510(k) premarket notification submitted by Data Medical Associates, Inc. for the device "DMA GLUCOSE HEXOKINASE U.V. PROCEDURE". The FDA issued a decision of Substantially Equivalent on October 3, 1995. The device falls under product code CFR (Hexokinase, Glucose), a Class II device regulated under 21 CFR 862.1345. Data Medical Associates, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 3, 1995
Date Received
May 25, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hexokinase, Glucose
Device Class
Class II
Regulation Number
862.1345
Review Panel
CH
Submission Type