Cleared Traditional

K903959 - NEONATAL METASCOPE

K903959 is an FDA 510(k) clearance for NEONATAL METASCOPE, manufactured by Cybermedic, Inc.. The device is a Class 2 Anesthesiology device with product code BZK cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K903959 · Cybermedic, Inc. · Anesthesiology device
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Nov 1990
Decision
87d
Days
Class 2
Risk

K903959 is an FDA 510(k) clearance for the NEONATAL METASCOPE. Classified as Spirometer, Monitoring (w/wo Alarm) (product code BZK), Class II - Special Controls.

Submitted by Cybermedic, Inc. (Washington, US). The FDA issued a Cleared decision on November 23, 1990 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1850 - 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 Cybermedic, Inc. devices

FDA 510(k) Submission Details - K903959

510(k) Number K903959 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 28, 1990
Decision Date November 23, 1990
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. No clinical trials required.

BZK Device Classification - Class 2, Special Controls

Product Code BZK Spirometer, Monitoring (w/wo Alarm)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1850
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 - BZK Spirometer, Monitoring (w/wo Alarm)

All 39
Devices cleared under the same product code (BZK) and FDA review panel - the closest regulatory comparables to K903959.
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS311
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K901885 · Bird Products Corp. · Sep 1990
MONAGHAN RVM, MODEL 761
K884942 · Monaghan Medical Corp. · Jun 1989
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K890724 · Bear Medical Systems, Inc. · Mar 1989