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510(k) K971157

MACRALP(A) ENZYME IMMUNOASSAY KIT by Strategic Diagnostics, Inc. — Product Code JHO

K971157 is an FDA 510(k) premarket notification submitted by Strategic Diagnostics, Inc. for the device "MACRALP(A) ENZYME IMMUNOASSAY KIT". The FDA issued a decision of Substantially Equivalent on April 15, 1998. The device falls under product code JHO (Electrophoretic Separation, Lipoproteins), a Class I device regulated under 21 CFR 862.1475.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 15, 1998
Date Received
March 28, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrophoretic Separation, Lipoproteins
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type

Other clearances for product code JHO

  • K022333 — SPIFE LIPPOROTEIN-12, MODEL 3344 (August 15, 2002)
  • K022053 — HYDRAGEL 7 LIPOPROTEIN(E), PN 4114 & HYDRAGEL LIPOPROTEIN(E) 15/30 PN 4134 (July 12, 2002)
  • K013662 — MODIFICATION TO LIPOPRINT SYSTEM, LDL SUBFRACTIONS (March 8, 2002)
  • K012789 — MODIFIED TO LDL/HDL CHOL DIRECT KIT-P.N. 4005, 4103,4123 (January 17, 2002)
  • K013466 — SPIFE 2000/3000 LIPOPROTEIN; MODEL# 3340, 3341, 3342, 3343 (December 21, 2001)
  • K010337 — LIPOPRINT SYSTEM, LDL SUBFRACTIONS (July 25, 2001)
  • K000603 — SPIFE CHOLESTEROL PROFILE KIT (April 17, 2000)
  • K992971 — REP CHOLESTEROL PROFILE KIT (October 18, 1999)
  • K974854 — HYDRAGEL-MINI LIPO KIT-PN 4093, HYDRAGEL LIPO KIT-PN 4007, HYDRAGEL LIPO MAXI KI (October 7, 1998)
  • K980650 — REP CHOLESTEROL PROFILE TEMPLATE-30, -16, -8; REP VIS CHOLESTEROL (May 1, 1998)

FDA data resources