Cleared Traditional

K790890 - TEMPO2-I DISPOSABLE THERMOMETERS (FDA 510(k) Clearance)

Class I General Hospital device.

K790890 · Airlife, Inc. · General Hospital
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Jun 1979
Decision
51d
Days
Class 1
Risk

K790890 is an FDA 510(k) clearance for the TEMPO2-I DISPOSABLE THERMOMETERS. Classified as Thermometer, Clinical Color Change (product code FQZ), Class I - General Controls.

Submitted by Airlife, Inc. (Walker, US). The FDA issued a Cleared decision on June 27, 1979 after a review of 51 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.2900 - the FDA general hospital 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 Airlife, Inc. devices

Submission Details

510(k) Number K790890 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 1979
Decision Date June 27, 1979
Days to Decision 51 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 128d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FQZ Thermometer, Clinical Color Change
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.2900
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.