Cleared Traditional

K780204 - CHEMISTRY CONTROL & REFERENCE SERUMS

K780204 is the FDA 510(k) clearance for CHEMISTRY CONTROL & REFERENCE SERUMS by Hyland Therapeutic Div., Travenol Laboratories. It is a Class 1 Chemistry device (product code JJT) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K780204 · Hyland Therapeutic Div., Travenol Laboratories · Chemistry device
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Mar 1978
Decision
24d
Days
Class 1
Risk

K780204 is an FDA 510(k) clearance for the CHEMISTRY CONTROL & REFERENCE SERUMS. Classified as Enzyme Controls (assayed And Unassayed) (product code JJT), Class I - General Controls.

Submitted by Hyland Therapeutic Div., Travenol Laboratories (Mchenry, US). The FDA issued a Cleared decision on March 3, 1978 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1660 - 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 Hyland Therapeutic Div., Travenol Laboratories devices

Submission Details

510(k) Number K780204 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 07, 1978
Decision Date March 03, 1978
Days to Decision 24 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
64d faster than avg
Panel avg: 88d · This submission: 24d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJT Enzyme Controls (assayed And Unassayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JJT Enzyme Controls (assayed And Unassayed)

All 58
Devices cleared under the same product code (JJT) and FDA review panel - the closest regulatory comparables to K780204.
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ISOZYME - ID CPK MARKER
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CLIN. CHEM. CONTROL SERUM-QUANTITATE
K780554 · Beckman Instruments, Inc. · Jun 1978
ISOENZYME SERUM CONTROL
K780147 · Corning Medical & Scientific · Feb 1978
ACA GLUTAMYL TRANSFERASE
K771800 · E.I. Dupont DE Nemours & Co., Inc. · Oct 1977
CARDIOZYME CK-CONTROL LEVEL 1
K771740 · Dade, Baxter Travenol Diagnostics, Inc. · Oct 1977