Cleared Traditional

K880411 - DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE

K880411 is an FDA 510(k) clearance for DEY-VIAL SODIUM CHLORIDE SOLUTION, manufactured by Dey Laboratories, Inc.. The device is a Class 2 Anesthesiology device with product code CAF cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K880411 · Dey Laboratories, Inc. · Anesthesiology device
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Feb 1988
Decision
28d
Days
Class 2
Risk

K880411 is an FDA 510(k) clearance for the DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE. Classified as Nebulizer (direct Patient Interface) (product code CAF), Class II - Special Controls.

Submitted by Dey Laboratories, Inc. (Concord, US). The FDA issued a Cleared decision on February 29, 1988 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5630 - 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 Dey Laboratories, Inc. devices

FDA 510(k) Submission Details - K880411

510(k) Number K880411 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 1988
Decision Date February 29, 1988
Days to Decision 28 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
112d faster than avg
Panel avg: 140d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CAF Device Classification - Class 2, Special Controls

Product Code CAF Nebulizer (direct Patient Interface)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5630
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 - CAF Nebulizer (direct Patient Interface)

All 248
Devices cleared under the same product code (CAF) and FDA review panel - the closest regulatory comparables to K880411.
INSPIRON NEBULO BASIC EXTERNAL HEATER
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ASTHMAKIT
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RESPIRGARD II NEBULIZER SYSTEM
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HOYER SOLVET
K873395 · Infrasonics Corp. · Oct 1987
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K871293 · Siemens Elema AB · May 1987