Cleared Traditional

K922007 - YSI MODEL 441A AIRWAY TEMPERATURE PROBE

K922007 is an FDA 510(k) clearance for YSI MODEL 441A AIRWAY TEMPERATURE PROBE, manufactured by Yellow Springs Instrument Co., Inc.. The device is a Class 2 Anesthesiology device with product code BZT cleared through the Traditional 510(k) pathway after a 188-day FDA review.

K922007 · Yellow Springs Instrument Co., Inc. · Anesthesiology device
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Nov 1992
Decision
188d
Days
Class 2
Risk

K922007 is an FDA 510(k) clearance for the YSI MODEL 441A AIRWAY TEMPERATURE PROBE. Classified as Stethoscope, Esophageal, With Electrical Conductors (product code BZT), Class II - Special Controls.

Submitted by Yellow Springs Instrument Co., Inc. (Yellow Springs, US). The FDA issued a Cleared decision on November 4, 1992 after a review of 188 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1920 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Yellow Springs Instrument Co., Inc. devices

FDA 510(k) Submission Details - K922007

510(k) Number K922007 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 1992
Decision Date November 04, 1992
Days to Decision 188 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
48d slower than avg
Panel avg: 140d · This submission: 188d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZT Device Classification - Class 2, Special Controls

Product Code BZT Stethoscope, Esophageal, With Electrical Conductors
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1920
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.

Regulatory Peers - BZT Stethoscope, Esophageal, With Electrical Conductors

All 18
Devices cleared under the same product code (BZT) and FDA review panel - the closest regulatory comparables to K922007.
Esophageal Stethoscope 9 French, Esophageal Stethoscope 12 French, Esophageal Stethoscope 18 French, Esophageal Stethoscope, 24 French
K193027 · Deroyal Industries, Inc. · Apr 2020
DEBUSK TEMPERATURE SYSTEMS PREMIER AND SIGNATURE SERIES MULTI-PURPOSE ESOPHAGEAL STETHOSCOPE
K940169 · Deroyal Industries, Inc. · Jul 1994
DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE
K925789 · Deroyal Industries, Inc. · Jul 1993
YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP
K893409 · Yellow Springs Instrument Co., Inc. · Jul 1989
TELEMETRIC STETHOSCOPE
K882319 · Vital Signs, Inc. · Aug 1988
SHERIDAN ELECTROSURGERY PROTECTION FILTER
K881293 · Sheridan Catheter Corp. · Jun 1988