Cleared Traditional

K790197 - REAGENT KIT

K790197 is the FDA 510(k) clearance for REAGENT KIT by Sherwood Medical Industries. It is a Class 1 Chemistry device (product code JJF) cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K790197 · Sherwood Medical Industries · Chemistry device
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Mar 1979
Decision
46d
Days
Class 1
Risk

K790197 is an FDA 510(k) clearance for the REAGENT KIT, LANCER GLUCOSE. Classified as Analyzer, Chemistry, Micro, For Clinical Use (product code JJF), Class I - General Controls.

Submitted by Sherwood Medical Industries (Mchenry, US). The FDA issued a Cleared decision on March 12, 1979 after a review of 46 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2170 - 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 Sherwood Medical Industries devices

Submission Details

510(k) Number K790197 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 1979
Decision Date March 12, 1979
Days to Decision 46 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 88d · This submission: 46d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJF Analyzer, Chemistry, Micro, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2170
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 - JJF Analyzer, Chemistry, Micro, For Clinical Use

All 32
Devices cleared under the same product code (JJF) and FDA review panel - the closest regulatory comparables to K790197.
WASH SOLUTION KIT, #88102
K802264 · Hi Chem, Inc. · Oct 1980
ELECTROLY TE CHEMISTRY ANALYZER
K802398 · Instrumentation Laboratory CO · Oct 1980
ASTRA PRINTER PAPER #88112-CHLORIDE SILV
K802392 · Hi Chem, Inc. · Oct 1980
BECKMAN ASTRA SYSTEM
K781442 · Beckman Instruments, Inc. · Oct 1978
STAC SYSTEM
K771821 · Technicon Instruments Corp. · Nov 1977
STAC SYSTEM-ADDI. ANALYTES
K771939 · Technicon Instruments Corp. · Nov 1977