Cleared Traditional

COMPLUS VARIOUS FORMS (K831039) - FDA 510(k) Clearance

K831039 · Parker Laboratories, Inc. · Dental device
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May 1983
Decision
57d
Days
-
Risk

K831039 is an FDA 510(k) clearance for the COMPLUS VARIOUS FORMS.

Submitted by Parker Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 27, 1983 after a review of 57 days - a notably fast clearance cycle.

This device falls under the Dental 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 Parker Laboratories, Inc. devices

Submission Details

510(k) Number K831039 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 1983
Decision Date May 27, 1983
Days to Decision 57 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 127d · This submission: 57d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -