Cleared Traditional

K884770 - ONCOPROBE SYSTEM

K884770 is an FDA 510(k) clearance for ONCOPROBE SYSTEM, manufactured by Care Wise Medical Products Corp.. The device is a Class 1 Radiology device with product code IZD cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K884770 · Care Wise Medical Products Corp. · Radiology device
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Jan 1989
Decision
51d
Days
Class 1
Risk

K884770 is an FDA 510(k) clearance for the ONCOPROBE SYSTEM. Classified as Probe, Uptake, Nuclear (product code IZD), Class I - General Controls.

Submitted by Care Wise Medical Products Corp. (Morgan Hill, US). The FDA issued a Cleared decision on January 4, 1989 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1320 - the FDA radiology and imaging software 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 Care Wise Medical Products Corp. devices

FDA 510(k) Submission Details - K884770

510(k) Number K884770 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1988
Decision Date January 04, 1989
Days to Decision 51 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 107d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

IZD Device Classification - Class 1, General Controls

Product Code IZD Probe, Uptake, Nuclear
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1320
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 - IZD Probe, Uptake, Nuclear

All 7
Devices cleared under the same product code (IZD) and FDA review panel - the closest regulatory comparables to K884770.
GAMMA GUIDANCE SYSTEM
K961321 · Radiation Monitoring Devices, Inc. · Feb 1997
NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
K962319 · Neoprobe Corp. · Sep 1996
THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME
K932153 · Biodan Medical Systems, Ltd. · Sep 1993
CARDIAC PROBE
K760595 · G.D. Searle and Co. · Sep 1976