Cleared Traditional

K984169 - DIGI-SNAP

K984169 is an FDA 510(k) clearance for DIGI-SNAP, manufactured by Snap Laboratories, LLC. The device is a Class 2 Anesthesiology device with product code MNR cleared through the Traditional 510(k) pathway after a 187-day FDA review.

K984169 · Snap Laboratories, LLC · Anesthesiology device
Download Printable Device Report (PDF)
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May 1999
Decision
187d
Days
Class 2
Risk

K984169 is an FDA 510(k) clearance for the DIGI-SNAP. Classified as Ventilatory Effort Recorder (product code MNR), Class II - Special Controls.

Submitted by Snap Laboratories, LLC (Glenview, US). The FDA issued a Cleared decision on May 26, 1999 after a review of 187 days - an extended review 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: 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 Snap Laboratories, LLC devices

FDA 510(k) Submission Details - K984169

510(k) Number K984169 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 1998
Decision Date May 26, 1999
Days to Decision 187 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
47d slower than avg
Panel avg: 140d · This submission: 187d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNR Device Classification - Class 2, Special Controls

Product Code MNR Ventilatory Effort Recorder
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 - MNR Ventilatory Effort Recorder

All 65
Devices cleared under the same product code (MNR) and FDA review panel - the closest regulatory comparables to K984169.
STARDUST II, MODEL 1011176
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APNOESCREEN PRO, ALPHA SCREEN PRO
K000396 · Erich Jaeger, Inc. · Dec 2000
SUZANNE
K990565 · Nellcor Puritan Bennett, Inc. · Aug 1999
SMARTRECORDER, MODEL 2500
K990199 · Respironics, Inc. · Apr 1999
STARDUST
K973920 · Respironics, Inc. · May 1998
SLEEPSCAN AIRFLOW PRESSURE TRANSDUCER
K971501 · Bio-Logic Systems Corp. · Oct 1997