Cleared Traditional

K965160 - HP ORVUE INTRA-OP (M2510A)

K965160 is an FDA 510(k) clearance for HP ORVUE INTRA-OP (M2510A), manufactured by Hewlett-Packard GmbH. The device is a Class 2 Anesthesiology device with product code BSZ cleared through the Traditional 510(k) pathway after a 262-day FDA review.

K965160 · Hewlett-Packard GmbH · Anesthesiology device
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Sep 1997
Decision
262d
Days
Class 2
Risk

K965160 is an FDA 510(k) clearance for the HP ORVUE INTRA-OP (M2510A). Classified as Gas-machine, Anesthesia (product code BSZ), Class II - Special Controls.

Submitted by Hewlett-Packard GmbH (Wuerttemberg, DE). The FDA issued a Cleared decision on September 11, 1997 after a review of 262 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 Hewlett-Packard GmbH devices

FDA 510(k) Submission Details - K965160

510(k) Number K965160 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 23, 1996
Decision Date September 11, 1997
Days to Decision 262 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
122d slower than avg
Panel avg: 140d · This submission: 262d
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 116
Devices cleared under the same product code (BSZ) and FDA review panel - the closest regulatory comparables to K965160.
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