Cleared Abbreviated

K991212 - MODIFICATION TO TRUZONE PEAK FLOW METER

K991212 is an FDA 510(k) clearance for MODIFICATION TO TRUZONE PEAK FLOW METER, manufactured by Monaghan Medical Corp.. The device is a Class 2 Anesthesiology device with product code BZH cleared through the Abbreviated 510(k) pathway after a 83-day FDA review.

K991212 · Monaghan Medical Corp. · Anesthesiology device
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Jul 1999
Decision
83d
Days
Class 2
Risk

K991212 is an FDA 510(k) clearance for the MODIFICATION TO TRUZONE PEAK FLOW METER. Classified as Meter, Peak Flow, Spirometry (product code BZH), Class II - Special Controls.

Submitted by Monaghan Medical Corp. (Plattsburgh, US). The FDA issued a Cleared decision on July 1, 1999 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1860 - the FDA anesthesiology and respiratory device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Monaghan Medical Corp. devices

FDA 510(k) Submission Details - K991212

510(k) Number K991212 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 09, 1999
Decision Date July 01, 1999
Days to Decision 83 days
Submission Type Abbreviated
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
57d faster than avg
Panel avg: 140d · This submission: 83d
Pathway characteristics
Standards-based clearance path.

BZH Device Classification - Class 2, Special Controls

Product Code BZH Meter, Peak Flow, Spirometry
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1860
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 - BZH Meter, Peak Flow, Spirometry

All 56
Devices cleared under the same product code (BZH) and FDA review panel - the closest regulatory comparables to K991212.
ONEFLOW
K980951 · Sti Medical · Feb 2000
VITALOGRAPH MICRO
K991412 · Vitalograph, Inc. · Feb 2000
RESPALERT
K992618 · Harwill Medical (Pty) , Ltd. · Oct 1999
AIRZONE PEAK FLOWMETER
K982334 · Clement Clarke Intl., Ltd. · Jan 1999
ACCUTRAX, MODEL EPF840
K982995 · Korr Medical Technologies, Inc. · Dec 1998
AIRWATCH II ZONELESS
K982675 · Enact Health Management Systems · Oct 1998