Cleared Traditional

K896070 - PFEIFFER METERED DOSAGE SYSTEM

K896070 is an FDA 510(k) clearance for PFEIFFER METERED DOSAGE SYSTEM, manufactured by Syva Co.. The device is a Class 1 Anesthesiology device with product code CCQ cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K896070 · Syva Co. · Anesthesiology device
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Jan 1990
Decision
90d
Days
Class 1
Risk

K896070 is an FDA 510(k) clearance for the PFEIFFER METERED DOSAGE SYSTEM. Classified as Nebulizer, Medicinal, Non-ventilatory (atomizer) (product code CCQ), Class I - General Controls.

Submitted by Syva Co. (Palo Alto, US). The FDA issued a Cleared decision on January 17, 1990 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5640 - 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 Syva Co. devices

FDA 510(k) Submission Details - K896070

510(k) Number K896070 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 19, 1989
Decision Date January 17, 1990
Days to Decision 90 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 140d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

CCQ Device Classification - Class 1, General Controls

Product Code CCQ Nebulizer, Medicinal, Non-ventilatory (atomizer)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5640
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 - CCQ Nebulizer, Medicinal, Non-ventilatory (atomizer)

All 18
Devices cleared under the same product code (CCQ) and FDA review panel - the closest regulatory comparables to K896070.
SALINE SOLUTION- STERILE
K922033 · Trinity Laboratories, Inc. · Jul 1992
MODIFIED AEROCHAMBER WITH MASK
K900576 · Monaghan Medical Corp. · May 1991
MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER
K900557 · Monaghan Medical Corp. · Apr 1991
DEVILBISS MODEL 6610D
K894441 · Devilbiss Health Care, Inc. · Oct 1989
DEVILBISS MODEL 8500D AND 8500D-608
K894244 · Devilbiss Health Care, Inc. · Oct 1989
MONAGHAN AEROCHAMBER WITH MASK
K874513 · Monaghan Medical Corp. · Dec 1987