Cleared Traditional

K905168 - HYPERLITE

K905168 is an FDA 510(k) clearance for HYPERLITE, manufactured by S.O.S. , Ltd.. The device is a Class 2 Anesthesiology device with product code CBF cleared through the Traditional 510(k) pathway after a 248-day FDA review.

K905168 · S.O.S. , Ltd. · Anesthesiology device
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Jul 1991
Decision
248d
Days
Class 2
Risk

K905168 is an FDA 510(k) clearance for the HYPERLITE. Classified as Chamber, Hyperbaric (product code CBF), Class II - Special Controls.

Submitted by S.O.S. , Ltd. (London Nw73js, England, GB). The FDA issued a Cleared decision on July 22, 1991 after a review of 248 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5470 - 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.

FDA 510(k) Submission Details - K905168

510(k) Number K905168 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 16, 1990
Decision Date July 22, 1991
Days to Decision 248 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
108d slower than avg
Panel avg: 140d · This submission: 248d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CBF Device Classification - Class 2, Special Controls

Product Code CBF Chamber, Hyperbaric
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5470
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 - CBF Chamber, Hyperbaric

All 60
Devices cleared under the same product code (CBF) and FDA review panel - the closest regulatory comparables to K905168.
LIFEFORCE CLINICAL HYPERBARIC FACILITY
K951125 · Reimers Systems, Inc. · Jun 1995
LAB-SITE(R) SAFETY CANNULA
K933929 · Migada, Ltd. · Dec 1993
SIGMA MP MULTIPLACE HYPERBARIC CHAMBER
K930748 · Perry Baromedical Services · Aug 1993
HYPERBARIC PENETRATION EXTENSION SET
K861315 · Cutter Laboratories, Inc. · May 1986
MICROSPAN -PH MONITOR
K842303 · Biochem International, Inc. · Oct 1984
K905168 · HYPERLITE
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