Cleared Traditional

K880979 - MARQUEST SCT 2000

K880979 is an FDA 510(k) clearance for MARQUEST SCT 2000, manufactured by Marquest Medical Products, Inc.. The device is a Class 2 Anesthesiology device with product code BTT cleared through the Traditional 510(k) pathway after a 129-day FDA review.

K880979 · Marquest Medical Products, Inc. · Anesthesiology device
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Jul 1988
Decision
129d
Days
Class 2
Risk

K880979 is an FDA 510(k) clearance for the MARQUEST SCT 2000, HEATED HUMIDIFICATION SYSTEM. Classified as Humidifier, Respiratory Gas, (direct Patient Interface) (product code BTT), Class II - Special Controls.

Submitted by Marquest Medical Products, Inc. (Englewood, US). The FDA issued a Cleared decision on July 15, 1988 after a review of 129 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5450 - 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 Marquest Medical Products, Inc. devices

FDA 510(k) Submission Details - K880979

510(k) Number K880979 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 08, 1988
Decision Date July 15, 1988
Days to Decision 129 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
11d faster than avg
Panel avg: 140d · This submission: 129d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTT Device Classification - Class 2, Special Controls

Product Code BTT Humidifier, Respiratory Gas, (direct Patient Interface)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5450
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 - BTT Humidifier, Respiratory Gas, (direct Patient Interface)

All 96
Devices cleared under the same product code (BTT) and FDA review panel - the closest regulatory comparables to K880979.
VHS 820 HUMIDIFIER, MODIFICATION
K893034 · Bear Medical Systems, Inc. · Jul 1989
MODEL MR2000 HEATED RESPIRATORY HUMIDIFIER
K881970 · Fisher &Paykel Healthcare , Ltd. · Mar 1989
STERILE INHALATION WATER TRANSFER SET
K882582 · Intertech Resources, Inc. · Sep 1988
BEAR VH-820 HUMIDIFIER
K873634 · Bear Medical Systems, Inc. · Dec 1987
STERILE WATER FOR INHALATION USP 2D0799
K851940 · Travenol Laboratories, S.A. · Jun 1985
VH820 HUMIDIFIER
K842340 · Bear Medical Systems, Inc. · Jul 1984