Cleared Traditional

K802600 - AMP PORTABLE PATIENT PRESSURE MONITOR

K802600 is the FDA 510(k) clearance for AMP PORTABLE PATIENT PRESSURE MONITOR by American Medical Products, Inc.. It is a Class 2 Cardiovascular device (product code DSK) cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K802600 · American Medical Products, Inc. · Cardiovascular device
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Nov 1980
Decision
22d
Days
Class 2
Risk

K802600 is an FDA 510(k) clearance for the AMP PORTABLE PATIENT PRESSURE MONITOR. Classified as Computer, Blood-pressure (product code DSK), Class II - Special Controls.

Submitted by American Medical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 12, 1980 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1110 - 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: 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 American Medical Products, Inc. devices

Submission Details

510(k) Number K802600 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 21, 1980
Decision Date November 12, 1980
Days to Decision 22 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 125d · This submission: 22d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DSK Computer, Blood-pressure
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1110
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DSK Computer, Blood-pressure

All 32
Devices cleared under the same product code (DSK) and FDA review panel - the closest regulatory comparables to K802600.
PRESSURE FUNCTION BLOCKS
K810172 · Honeywell, Inc. · Feb 1981
PATIENT MONITOR CM111, 112
K810178 · Honeywell, Inc. · Feb 1981
DUAL TRACE PATIENT MONITOR 116,118,120
K810179 · Honeywell, Inc. · Feb 1981
PRESSURE MONITOR, MODEL 1131B
K801110 · American Optical Corp. · May 1980
MODEL 1981 PRESSUROMETER DATA ANALYSIS
K792077 · Del Mar Avionics · Dec 1979
MONITOR, PRESSURVEIL
K790135 · Concept, Inc. · Feb 1979