Cleared Traditional

K800850 - HIGH STOY SMALL PARTS SCANNER #SP-100B

K800850 is an FDA 510(k) clearance for HIGH STOY SMALL PARTS SCANNER #SP-100B, manufactured by Highstoy. The device is a Class 2 Cardiovascular device with product code DXK cleared through the Traditional 510(k) pathway after a 97-day FDA review.

K800850 · Highstoy · Cardiovascular device
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Jul 1980
Decision
97d
Days
Class 2
Risk

K800850 is an FDA 510(k) clearance for the HIGH STOY SMALL PARTS SCANNER #SP-100B. Classified as Echocardiograph (product code DXK), Class II - Special Controls.

Submitted by Highstoy (Mchenry, US). The FDA issued a Cleared decision on July 21, 1980 after a review of 97 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2330 - 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 Highstoy devices

FDA 510(k) Submission Details - K800850

510(k) Number K800850 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1980
Decision Date July 21, 1980
Days to Decision 97 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
28d faster than avg
Panel avg: 125d · This submission: 97d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXK Device Classification - Class 2, Special Controls

Product Code DXK Echocardiograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2330
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 - DXK Echocardiograph

All 47
Devices cleared under the same product code (DXK) and FDA review panel - the closest regulatory comparables to K800850.
U.I. OCTOSON
K802030 · Ausonics Pty , Ltd. · Oct 1980
ULTRA IMAGER
K800553 · Honeywell, Inc. · Jul 1980
LINEAR ARRAY SCANNER
K800805 · Philips Medical Systems (Cleveland), Inc. · Jul 1980
IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA-
K792373 · Ipco Corp. · Feb 1980
CATHODE RAY TUBE DISPLAY MODEL 1340A
K780332 · Hewlett-Packard Co. · Mar 1978
HIGH-SPEED SECTOR SCANNING SSL-52H
K771292 · Toshiba Medical Systems · Aug 1977