Cleared Traditional

K770883 - ULTRAZYME PLUS GOT (FDA 510(k) Clearance)

K770883 · Harleco · Chemistry device
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Jul 1977
Decision
59d
Days
-
Risk

K770883 is an FDA 510(k) clearance for the ULTRAZYME PLUS GOT.

Submitted by Harleco (Mchenry, US). The FDA issued a Cleared decision on July 14, 1977 after a review of 59 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 Harleco devices

Submission Details

510(k) Number K770883 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 16, 1977
Decision Date July 14, 1977
Days to Decision 59 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
29d faster than avg
Panel avg: 88d · This submission: 59d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -