Cleared Traditional

K861669 - SODIUM, POTASSIUM AND CHLORIDE PROCEDURE

K861669 is an FDA 510(k) clearance for SODIUM, manufactured by Data Medical Associates, Inc.. The device is a Class 2 Chemistry device with product code CGZ cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K861669 · Data Medical Associates, Inc. · Chemistry device
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May 1986
Decision
27d
Days
Class 2
Risk

K861669 is an FDA 510(k) clearance for the SODIUM, POTASSIUM AND CHLORIDE PROCEDURE. Classified as Electrode, Ion-specific, Chloride (product code CGZ), Class II - Special Controls.

Submitted by Data Medical Associates, Inc. (Arlington, US). The FDA issued a Cleared decision on May 27, 1986 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1170 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Data Medical Associates, Inc. devices

FDA 510(k) Submission Details - K861669

510(k) Number K861669 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 1986
Decision Date May 27, 1986
Days to Decision 27 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
61d faster than avg
Panel avg: 88d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CGZ Device Classification - Class 2, Special Controls

Product Code CGZ Electrode, Ion-specific, Chloride
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1170
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 - CGZ Electrode, Ion-specific, Chloride

All 35
Devices cleared under the same product code (CGZ) and FDA review panel - the closest regulatory comparables to K861669.
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