Cleared Traditional

K810091 - GLUCOSE STANDARD

K810091 is an FDA 510(k) clearance for GLUCOSE STANDARD, manufactured by Anco Medical Reagents & Assoc.. The device is a Class 2 Chemistry device with product code JIS cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K810091 · Anco Medical Reagents & Assoc. · Chemistry device
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Jan 1981
Decision
13d
Days
Class 2
Risk

K810091 is an FDA 510(k) clearance for the GLUCOSE STANDARD. Classified as Calibrator, Primary (product code JIS), Class II - Special Controls.

Submitted by Anco Medical Reagents & Assoc. (Mchenry, US). The FDA issued a Cleared decision on January 26, 1981 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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 Anco Medical Reagents & Assoc. devices

FDA 510(k) Submission Details - K810091

510(k) Number K810091 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 13, 1981
Decision Date January 26, 1981
Days to Decision 13 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
75d faster than avg
Panel avg: 88d · This submission: 13d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JIS Device Classification - Class 2, Special Controls

Product Code JIS Calibrator, Primary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
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 - JIS Calibrator, Primary

All 112
Devices cleared under the same product code (JIS) and FDA review panel - the closest regulatory comparables to K810091.
LECITHIN-SPINGOMYELIN STAND. & KITS
K810743 · Supelco, Inc. · Mar 1981
EMIT-TFG PRISMA THYROXINE CALIBRATORS
K810587 · Syva Co. · Mar 1981
CHOLESTEROL STANDARD
K810092 · Anco Medical Reagents & Assoc. · Feb 1981
CREATININE STANDARDS
K802631 · Gilford Diagnostics · Dec 1980
UV URIC ACID STANDARDS
K801501 · The Dow Chemical Co. · Sep 1980
SERALYZER GLUCOSE CALIBRATORS(LOW&HIGH)
K801665 · Miles Laboratories, Inc. · Aug 1980