Cleared Traditional

K801184 - CONPHAR SPRAGUE RAPPAPORT STETHOSCOPE

K801184 is an FDA 510(k) clearance for CONPHAR SPRAGUE RAPPAPORT STETHOSCOPE, manufactured by Conphar, Inc.. The device is a Class 1 Cardiovascular device with product code LDE cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K801184 · Conphar, Inc. · Cardiovascular device
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Jun 1980
Decision
19d
Days
Class 1
Risk

K801184 is an FDA 510(k) clearance for the CONPHAR SPRAGUE RAPPAPORT STETHOSCOPE. Classified as Stethoscope, Manual (product code LDE), Class I - General Controls.

Submitted by Conphar, Inc. (Walker, US). The FDA issued a Cleared decision on June 4, 1980 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1875 - 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 Conphar, Inc. devices

FDA 510(k) Submission Details - K801184

510(k) Number K801184 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 16, 1980
Decision Date June 04, 1980
Days to Decision 19 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
106d faster than avg
Panel avg: 125d · This submission: 19d
Pathway characteristics
Predicate-based equivalence.

LDE Device Classification - Class 1, General Controls

Product Code LDE Stethoscope, Manual
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 870.1875
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 - LDE Stethoscope, Manual

All 7
Devices cleared under the same product code (LDE) and FDA review panel - the closest regulatory comparables to K801184.
VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:
K871369 · Keeler Instruments, Inc. · Sep 1987
LITTMAN TUNABLE STETHOSCOPE 2136
K821909 · 3M Company · Jul 1982
CONPHAR DUAL HEAD STETHOSCOPE
K801183 · Conphar, Inc. · Jun 1980
CONPHAR BOWLS STETHOSCOPE
K801185 · Conphar, Inc. · Jun 1980
ABCO PEDIATRIC STETHOSCOPE
K801215 · Abco Dealers, Inc. · Jun 1980