Cleared Traditional

K820190 - CALIBRATOR SET

K820190 is the FDA 510(k) clearance for CALIBRATOR SET by Syva Co.. It is a Class 2 Toxicology device (product code DKB) cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K820190 · Syva Co. · Toxicology device
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Feb 1982
Decision
18d
Days
Class 2
Risk

K820190 is an FDA 510(k) clearance for the CALIBRATOR SET. Classified as Calibrators, Drug Mixture (product code DKB), Class II - Special Controls.

Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on February 12, 1982 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3200 - the FDA toxicology device 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 Syva Co. devices

Submission Details

510(k) Number K820190 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 1982
Decision Date February 12, 1982
Days to Decision 18 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 87d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DKB Calibrators, Drug Mixture
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3200
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 Toxicology devices follow this clearance model.

Regulatory Peers - DKB Calibrators, Drug Mixture

All 77
Devices cleared under the same product code (DKB) and FDA review panel - the closest regulatory comparables to K820190.
ADVANCE SYSTEM EMITAED ANTIEPILEPTIC
K823740 · Syva Co. · Jan 1983
EMIT ST URINE METHAGUALONE CALIBRATOR
K821767 · Syva Co. · Jun 1982
EMIT-ST URINE CALIBRATOR A (#3A319
K820461 · Syva Co. · Mar 1982
EMIT-TOX SERUM CALIBRATORS
K811620 · Syva Co. · Jun 1981
EMIT-ST SERUM CALBRATOR
K810464 · Syva Co. · Mar 1981
EMIT-STM URINE CALIBRATORS
K802624 · Syva Co. · Nov 1980