Cleared Traditional

PHOTOVOLT PVA 4M+2 ANALYZER (K800453) - FDA 510(k) Clearance

Class I Chemistry device.

Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1980
Decision
20d
Days
Class 1
Risk

K800453 is an FDA 510(k) clearance for the PHOTOVOLT PVA 4M+2 ANALYZER. Classified as Analyzer, Chemistry (sequential Multiple, Continuous Flow) Clinical Use (product code JJC), Class I - General Controls.

Submitted by Photovolt Corp. (Mchenry, US). The FDA issued a Cleared decision on March 20, 1980 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2150 - 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 Photovolt Corp. devices

Submission Details

510(k) Number K800453 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 29, 1980
Decision Date March 20, 1980
Days to Decision 20 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 88d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJC Analyzer, Chemistry (sequential Multiple, Continuous Flow) Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2150
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 - JJC Analyzer, Chemistry (sequential Multiple, Continuous Flow) Clinical Use

All 16
Devices cleared under the same product code (JJC) and FDA review panel - the closest regulatory comparables to K800453.
TECHNICON RA-1000 SYSTEM
K833023 · Technicon Instruments Corp. · Nov 1983
TECHNICON SMAC II SYSTEM & ACCESSORIES
K811249 · Technicon Instruments Corp. · May 1981
BMC RIAFLO SYSTEM
K801481 · Boehringer Mannheim Corp. · Aug 1980
TECHNICON C800 SYSTEM
K792285 · Technicon Instruments Corp. · Dec 1979
TECHNICON STAT/LYTE ISE ELECTROLYTE
K781503 · Technicon Instruments Corp. · Sep 1978
SMA II
K771336 · Technicon Instruments Corp. · Aug 1977