Cleared Traditional

K992823 - SPIROVIT SP-2, PNEUMOCHECK II

K992823 is an FDA 510(k) clearance for SPIROVIT SP-2, manufactured by Schiller AG. The device is a Class 2 Anesthesiology device with product code BZG cleared through the Traditional 510(k) pathway after a 263-day FDA review.

K992823 · Schiller AG · Anesthesiology device
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May 2000
Decision
263d
Days
Class 2
Risk

K992823 is an FDA 510(k) clearance for the SPIROVIT SP-2, PNEUMOCHECK II. Classified as Spirometer, Diagnostic (product code BZG), Class II - Special Controls.

Submitted by Schiller AG (Baar, CH). The FDA issued a Cleared decision on May 12, 2000 after a review of 263 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1840 - 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 Schiller AG devices

FDA 510(k) Submission Details - K992823

510(k) Number K992823 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 23, 1999
Decision Date May 12, 2000
Days to Decision 263 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
123d slower than avg
Panel avg: 140d · This submission: 263d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZG Device Classification - Class 2, Special Controls

Product Code BZG Spirometer, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1840
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 - BZG Spirometer, Diagnostic

All 152
Devices cleared under the same product code (BZG) and FDA review panel - the closest regulatory comparables to K992823.
BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE
K002499 · Brentwood Medical Technology Corp. · Nov 2000
VITALOGRAPH BASE STATION
K000599 · Vitalograph, Inc. · Sep 2000
NDD MEDICAL TECHNOLOGIES EASYONE SPIROMETER: FRONTLINE MODEL 2000 AND DIAGNOSTIC MODEL 2001
K993921 · Ndd Medical Technologies · May 2000
COLLINS CPL
K992743 · Collins Medical, Inc. · Sep 1999
SPIROVIT, MODEL SP-250
K984031 · Schiller AG · Apr 1999
MIR SPIROBANK SPIROMETER
K983909 · Mir Medical Intl. Research Srl · Dec 1998