Cleared Traditional

K812308 - LANCER BUN RATE REAGENT KIT

K812308 is an FDA 510(k) clearance for LANCER BUN RATE REAGENT KIT, manufactured by Sherwood Medical Co.. The device is a Class 2 Chemistry device with product code CDS cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K812308 · Sherwood Medical Co. · Chemistry device
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Aug 1981
Decision
14d
Days
Class 2
Risk

K812308 is an FDA 510(k) clearance for the LANCER BUN RATE REAGENT KIT. Classified as Electrode, Ion Specific, Urea Nitrogen (product code CDS), Class II - Special Controls.

Submitted by Sherwood Medical Co. (Mchenry, US). The FDA issued a Cleared decision on August 31, 1981 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1770 - 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 Co. devices

FDA 510(k) Submission Details - K812308

510(k) Number K812308 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 1981
Decision Date August 31, 1981
Days to Decision 14 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
74d faster than avg
Panel avg: 88d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CDS Device Classification - Class 2, Special Controls

Product Code CDS Electrode, Ion Specific, Urea Nitrogen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1770
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CDS Electrode, Ion Specific, Urea Nitrogen

All 9
Devices cleared under the same product code (CDS) and FDA review panel - the closest regulatory comparables to K812308.
epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test
K171247 · Epocal, Inc. · Jan 2018
BUN REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA REAGENT
K033056 · Diamond Diagnostics, Inc. · Jan 2004
HI CHEM BUN REAGENT KIT,PRODUCT NUMBER 88806
K925550 · Hichem Diagnostics · Apr 1993
BUN REAGENT KIT #88108
K800616 · Hi Chem, Inc. · Apr 1980
BUN KIT
K800590 · Nobel Scientific Industries, Inc. · Apr 1980
BUN REAGENT KIT
K800071 · Fisher Scientific Co., LLC · Feb 1980