Cleared Traditional

K781217 - DATA TERMINAL MODEL 722

K781217 is the FDA 510(k) clearance for DATA TERMINAL MODEL 722 by Corning Medical & Scientific. It is a Class 1 Chemistry device (product code JQP) cleared through the Traditional 510(k) pathway after a 35-day FDA review.

K781217 · Corning Medical & Scientific · Chemistry device
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Aug 1978
Decision
35d
Days
Class 1
Risk

K781217 is an FDA 510(k) clearance for the DATA TERMINAL MODEL 722. Classified as Calculator/data Processing Module, For Clinical Use (product code JQP), Class I - General Controls.

Submitted by Corning Medical & Scientific (Mchenry, US). The FDA issued a Cleared decision on August 21, 1978 after a review of 35 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2100 - the FDA in vitro diagnostics and chemistry 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 Corning Medical & Scientific devices

Submission Details

510(k) Number K781217 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 17, 1978
Decision Date August 21, 1978
Days to Decision 35 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 88d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JQP Calculator/data Processing Module, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2100
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 - JQP Calculator/data Processing Module, For Clinical Use

All 48
Devices cleared under the same product code (JQP) and FDA review panel - the closest regulatory comparables to K781217.
PROCESSOR, K750 COMPUTER/DATA
K782052 · Kallestad Laboratories, Inc. · Jan 1979
EMIT MCA PROGRAM TAPE
K781081 · Instrumentation Laboratory CO · Sep 1978
COMPUTER INTERFACE IL 814
K781173 · Instrumentation Laboratory CO · Sep 1978
EMIT CLINICAL PROCESSOR - CP 5000
K780881 · Syva Co. · Jun 1978
DATA REDUCTION SYSTEM, DP-3000
K770877 · Beckman Instruments, Inc. · Jul 1977
GAMMACORD II CALCULATOR INTERFACE
K761063 · Miles Laboratories, Inc. · Dec 1976