Cleared Traditional

K812667 - MEDDARS/ULTRA IMAGER RESPIRATION MODULE

K812667 is an FDA 510(k) clearance for MEDDARS/ULTRA IMAGER RESPIRATION MODULE, manufactured by Honeywell, Inc.. The device is a Class 2 Anesthesiology device with product code BZQ cleared through the Traditional 510(k) pathway after a 32-day FDA review.

K812667 · Honeywell, Inc. · Anesthesiology device
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Oct 1981
Decision
32d
Days
Class 2
Risk

K812667 is an FDA 510(k) clearance for the MEDDARS/ULTRA IMAGER RESPIRATION MODULE. Classified as Monitor, Breathing Frequency (product code BZQ), Class II - Special Controls.

Submitted by Honeywell, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 23, 1981 after a review of 32 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.2375 - 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 Honeywell, Inc. devices

FDA 510(k) Submission Details - K812667

510(k) Number K812667 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 21, 1981
Decision Date October 23, 1981
Days to Decision 32 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
108d faster than avg
Panel avg: 140d · This submission: 32d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZQ Device Classification - Class 2, Special Controls

Product Code BZQ Monitor, Breathing Frequency
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.2375
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 - BZQ Monitor, Breathing Frequency

All 65
Devices cleared under the same product code (BZQ) and FDA review panel - the closest regulatory comparables to K812667.
TRIMED 510 APNEA MONITOR
K822819 · Tri-Med, Inc. · Nov 1982
HEALTHDYNE MODEL 16900 INFANT MONITOR
K821731 · Healthdyne, Inc. · Jul 1982
INFANT MONITOR
K820645 · Healthdyne, Inc. · Apr 1982
NEO NATAL RESPIRATION FUNCTION BLOCK
K810175 · Honeywell, Inc. · Mar 1981
RESPIRATION FUNCTION BLOCKS
K810174 · Honeywell, Inc. · Mar 1981
ECG/RESPIRATION STIMULATOR
K802205 · Healthdyne, Inc. · Oct 1980