Cleared Traditional

K790185 - MODEL V 4207 INTEGRATING PLUG-IN (FDA 510(k) Clearance)

Class II Anesthesiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K790185 · Electronics For Medicine, Inc. · Anesthesiology device
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Feb 1979
Decision
18d
Days
Class 2
Risk

K790185 is an FDA 510(k) clearance for the MODEL V 4207 INTEGRATING PLUG-IN. Classified as Calculator, Pulmonary Function Data (product code BZC), Class II - Special Controls.

Submitted by Electronics For Medicine, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 16, 1979 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1880 - the FDA anesthesiology and respiratory device 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 Electronics For Medicine, Inc. devices

Submission Details

510(k) Number K790185 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 1979
Decision Date February 16, 1979
Days to Decision 18 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
121d faster than avg
Panel avg: 139d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code BZC Calculator, Pulmonary Function Data
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1880
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 Anesthesiology devices follow this clearance model.