Cleared Traditional

K870362 - CALCIUM REAGENT - CRESOLPHTHALEIN COMPL...

K870362 is the FDA 510(k) clearance for CALCIUM REAGENT - CRESOLPHTHALEIN COMPL... by Trace Scientific , Ltd.. It is a Class 2 Chemistry device (product code CIC) cleared through the Traditional 510(k) pathway after a 205-day FDA review.

K870362 · Trace Scientific , Ltd. · Chemistry device
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Aug 1987
Decision
205d
Days
Class 2
Risk

K870362 is an FDA 510(k) clearance for the CALCIUM REAGENT - CRESOLPHTHALEIN COMPLEXON METHOD. Classified as Cresolphthalein Complexone, Calcium (product code CIC), Class II - Special Controls.

Submitted by Trace Scientific , Ltd. (Clayton, Vic 3168, AU). The FDA issued a Cleared decision on August 21, 1987 after a review of 205 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1145 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Trace Scientific , Ltd. devices

Submission Details

510(k) Number K870362 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 28, 1987
Decision Date August 21, 1987
Days to Decision 205 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
117d slower than avg
Panel avg: 88d · This submission: 205d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CIC Cresolphthalein Complexone, Calcium
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1145
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CIC Cresolphthalein Complexone, Calcium

All 67
Devices cleared under the same product code (CIC) and FDA review panel - the closest regulatory comparables to K870362.
PARAMAX CALCIUM REAGENT
K873519 · Baxter Healthcare Corp · Dec 1987
CRESOLPHTHALEIN COMPLEXONE, CALCIUM
K874131 · Pointe Scientific, Inc., · Dec 1987
WAKO(TM) AUTOKIT CALCIUM
K873334 · Wako Chemicals USA, Inc. · Oct 1987
SYSTEM PACK FOR B.M.D/HITACHI 704 CHEM. ANA.(GABA)
K872306 · Boehringer Mannheim Corp. · Aug 1987
SIGMA'S CALCIUM PROCEDURE NO. 587
K871152 · Sigma Diagnostics, Inc. · Jun 1987
SYSTEM REAGENTS HITACHI 737 CALCIUM (EDTA)
K871811 · Boehringer Mannheim Corp. · May 1987