Cleared Traditional

REAGENTS FOR QUANT. ENZYMATIC DETER.-TR. (K810951) - FDA 510(k) Clearance

K810951 · Mid Tech, Inc. · Chemistry device
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Apr 1981
Decision
16d
Days
-
Risk

K810951 is an FDA 510(k) clearance for the REAGENTS FOR QUANT. ENZYMATIC DETER.-TR..

Submitted by Mid Tech, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 23, 1981 after a review of 16 days - a notably fast clearance cycle.

This device falls under the Chemistry 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 Mid Tech, Inc. devices

Submission Details

510(k) Number K810951 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1981
Decision Date April 23, 1981
Days to Decision 16 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 88d · This submission: 16d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -