Cleared Traditional

K791302 - MANUAL MICRO ELISA READER #2-530

K791302 is the FDA 510(k) clearance for MANUAL MICRO ELISA READER #2-530 by Dynatech Laboratories, Inc.. It is a Class 1 Chemistry device (product code JJQ) cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K791302 · Dynatech Laboratories, Inc. · Chemistry device
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Aug 1979
Decision
37d
Days
Class 1
Risk

K791302 is an FDA 510(k) clearance for the MANUAL MICRO ELISA READER #2-530. Classified as Colorimeter, Photometer, Spectrophotometer For Clinical Use (product code JJQ), Class I - General Controls.

Submitted by Dynatech Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 16, 1979 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2300 - 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 Dynatech Laboratories, Inc. devices

Submission Details

510(k) Number K791302 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 10, 1979
Decision Date August 16, 1979
Days to Decision 37 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
51d faster than avg
Panel avg: 88d · This submission: 37d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2300
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 - JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

All 134
Devices cleared under the same product code (JJQ) and FDA review panel - the closest regulatory comparables to K791302.
MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.
K800523 · Varian Assoc., Inc. · Mar 1980
MICRO ELISA MINI READER
K800057 · Dynatech Laboratories, Inc. · Feb 1980
AMES DEXTROMETER REFLECTANCE COLORIMETER
K792292 · Miles Laboratories, Inc. · Dec 1979
CARY 210 SERIES, SPECTROPHOTOMETER
K791102 · Varian Assoc., Inc. · Jul 1979
MULTISKAN (78-503-00)
K790422 · Flow Laboratories, Inc. · Apr 1979
HEMESPEC
K782035 · Helena Laboratories · Jan 1979