Cleared Traditional

MICRO DELTA & CELTAPRO (K841964) - FDA 510(k) Clearance

Class I Radiology device.

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Aug 1984
Decision
99d
Days
Class 1
Risk

K841964 is an FDA 510(k) clearance for the MICRO DELTA & CELTAPRO. Classified as Camera, Scintillation (gamma) (product code IYX), Class I - General Controls.

Submitted by Computer Design & Applications, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 21, 1984 after a review of 99 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1100 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Computer Design & Applications, Inc. devices

Submission Details

510(k) Number K841964 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 14, 1984
Decision Date August 21, 1984
Days to Decision 99 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
8d faster than avg
Panel avg: 107d · This submission: 99d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code IYX Camera, Scintillation (gamma)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1100
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 - IYX Camera, Scintillation (gamma)

All 29
Devices cleared under the same product code (IYX) and FDA review panel - the closest regulatory comparables to K841964.
CX250 MOBILE GAMMA CAMERA & DCS CONSOLE
K880878 · Philips Medical Systems (Cleveland), Inc. · Sep 1988
STARPORT MODEL H3300AA
K852648 · General Electric Co. · Jan 1986
TOMOGRAPHIC GANTRY
K844218 · General Electric Co. · Mar 1985
MAXICAMERA 400 AC
K841906 · General Electric Co. · Jul 1984
ADD'L TERMINAL SUPPORT FOR STAR BASIC
K820244 · General Electric Co. · Mar 1982
DYNA- MO
K811629 · Philips Medical Systems (Cleveland), Inc. · Sep 1981