Cleared Traditional

K894642 - SLEEPAP MASK

K894642 is an FDA 510(k) clearance for SLEEPAP MASK, manufactured by Medical Industries America, Inc.. The device is a Class 1 Anesthesiology device with product code BYG cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K894642 · Medical Industries America, Inc. · Anesthesiology device
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Oct 1989
Decision
87d
Days
Class 1
Risk

K894642 is an FDA 510(k) clearance for the SLEEPAP MASK. Classified as Mask, Oxygen (product code BYG), Class I - General Controls.

Submitted by Medical Industries America, Inc. (West Des Moines, US). The FDA issued a Cleared decision on October 19, 1989 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5580 - 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 Medical Industries America, Inc. devices

FDA 510(k) Submission Details - K894642

510(k) Number K894642 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1989
Decision Date October 19, 1989
Days to Decision 87 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 140d · This submission: 87d
Pathway characteristics
Predicate-based equivalence.

BYG Device Classification - Class 1, General Controls

Product Code BYG Mask, Oxygen
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5580
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - BYG Mask, Oxygen

All 19
Devices cleared under the same product code (BYG) and FDA review panel - the closest regulatory comparables to K894642.
SEAL RING FOR NASAL CPAP
K921499 · Devilbiss Health Care, Inc. · Sep 1992
SALTER LABS INFANT MEDIUM CONCENTRATION MASK
K912633 · Salter Labs · Jul 1991
KENDALL CURITY OXYGEN MASK
K892434 · The Kendal Co. · Aug 1989
SINGLE PATIENT USE NASAL (CPAP) CIRCUIT
K890193 · Puritan Bennett Corp. · Mar 1989
MASK, OXYGEN
K874092 · Life Support Products, Inc. · Feb 1988
SALTER LABS #4004/4104 OXYGEN MASK W/C02 SAMP LINE
K865047 · Salter Labs · Feb 1987