510(k) K930166

IRON TEST #'S 42376/93,42324/R1A,42324/R1B,42324/R by Em Diagnostic Systems, Inc. — Product Code JIY

K930166 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "IRON TEST #'S 42376/93,42324/R1A,42324/R1B,42324/R". The FDA issued a decision of Substantially Equivalent on April 21, 1993. The device falls under product code JIY (Photometric Method, Iron (Non-Heme)), a Class I device regulated under 21 CFR 862.1410. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 1993
Date Received
January 13, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Photometric Method, Iron (Non-Heme)
Device Class
Class I
Regulation Number
862.1410
Review Panel
CH
Submission Type