Cleared Traditional

SDI PREPAX DILUKIT CA (K840042) - FDA 510(k) Clearance

K840042 · Scientific Distributors, Inc. · Hematology device
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Feb 1984
Decision
35d
Days
-
Risk

K840042 is an FDA 510(k) clearance for the SDI PREPAX DILUKIT CA.

Submitted by Scientific Distributors, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 10, 1984 after a review of 35 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel. 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 Scientific Distributors, Inc. devices

Submission Details

510(k) Number K840042 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 06, 1984
Decision Date February 10, 1984
Days to Decision 35 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 113d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -