Cleared Traditional

K062388 - ANESTHESIA INFORMATION AND DIGITAL-DRUG...

K062388 is an FDA 510(k) clearance for ANESTHESIA INFORMATION AND DIGITAL-DRUG..., manufactured by Docusys. The device is a Class 2 Anesthesiology device with product code BSZ cleared through the Traditional 510(k) pathway after a 191-day FDA review.

K062388 · Docusys · Anesthesiology device
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Optimized for regulatory review, auditing and printing
Feb 2007
Decision
191d
Days
Class 2
Risk

K062388 is an FDA 510(k) clearance for the ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM. Classified as Gas-machine, Anesthesia (product code BSZ), Class II - Special Controls.

Submitted by Docusys (Mobile, US). The FDA issued a Cleared decision on February 22, 2007 after a review of 191 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5160 - 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 Docusys devices

FDA 510(k) Submission Details - K062388

510(k) Number K062388 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 15, 2006
Decision Date February 22, 2007
Days to Decision 191 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
51d slower than avg
Panel avg: 140d · This submission: 191d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BSZ Device Classification - Class 2, Special Controls

Product Code BSZ Gas-machine, Anesthesia
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5160
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 - BSZ Gas-machine, Anesthesia

All 115
Devices cleared under the same product code (BSZ) and FDA review panel - the closest regulatory comparables to K062388.
GE DATEX-OHMEDA AISYS
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K061609 · Datex-Ohmeda, Inc. · Jun 2006
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K050676 · Datex-Ohmeda, Inc. · Apr 2005
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K050626 · Datex-Ohmeda, Inc. · Mar 2005