Cleared Traditional

K831134 - PHOENIX 60/60 PROCESSOR MODULE

K831134 is an FDA 510(k) clearance for PHOENIX 60/60 PROCESSOR MODULE, manufactured by Phoenix Corp.. The device is a Class 1 Cardiovascular device with product code DSF cleared through the Traditional 510(k) pathway after a 214-day FDA review.

K831134 · Phoenix Corp. · Cardiovascular device
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Nov 1983
Decision
214d
Days
Class 1
Risk

K831134 is an FDA 510(k) clearance for the PHOENIX 60/60 PROCESSOR MODULE. Classified as Recorder, Paper Chart (product code DSF), Class I - General Controls.

Submitted by Phoenix Corp. (Mchenry, US). The FDA issued a Cleared decision on November 7, 1983 after a review of 214 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2810 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Phoenix Corp. devices

FDA 510(k) Submission Details - K831134

510(k) Number K831134 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1983
Decision Date November 07, 1983
Days to Decision 214 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
89d slower than avg
Panel avg: 125d · This submission: 214d
Pathway characteristics
Predicate-based equivalence.

DSF Device Classification - Class 1, General Controls

Product Code DSF Recorder, Paper Chart
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 870.2810
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 - DSF Recorder, Paper Chart

All 57
Devices cleared under the same product code (DSF) and FDA review panel - the closest regulatory comparables to K831134.
2-CHANNEL RECORDER
K832998 · Litton Medical Electronics · Jun 1984
I-CHANNEL RECORDER
K833000 · Litton Medical Electronics · Jun 1984
MONITORING SYSTEM AS100-AS115 RECORD
K832754 · Air-Shields, Inc. · Dec 1983
MEDICAL ELECTRONICS-PRINTER CLOCK
K832012 · Litton Medical Electronics · Oct 1983
DUAL CHANNEL RECORDER #78574A
K830315 · Hewlett-Packard Co. · Mar 1983
MINGOGRAF 4, MINGO CARD 4 & MINOCARD 3
K822978 · Siemens Corp. · Dec 1982