510(k) K040025

A1C-CELLULAR by Streck Laboratories, Inc. — Product Code JJX

K040025 is an FDA 510(k) premarket notification submitted by Streck Laboratories, Inc. for the device "A1C-CELLULAR". The FDA issued a decision of Substantially Equivalent on March 2, 2004. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Streck Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 2, 2004
Date Received
January 7, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Single (Specified) Analyte Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type