Cleared Traditional

K082087 - EYEFEEL OPHTHALMIC WARMER

K082087 is an FDA 510(k) clearance for EYEFEEL OPHTHALMIC WARMER, manufactured by Bio-Lipid, Inc.. The device is a Class 1 Physical Medicine device with product code IMD cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K082087 · Bio-Lipid, Inc. · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 2008
Decision
50d
Days
Class 1
Risk

K082087 is an FDA 510(k) clearance for the EYEFEEL OPHTHALMIC WARMER. Classified as Pack, Hot Or Cold, Disposable (product code IMD), Class I - General Controls.

Submitted by Bio-Lipid, Inc. (Washington, US). The FDA issued a Cleared decision on September 11, 2008 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5710 - the FDA physical medicine 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.

FDA 510(k) Submission Details - K082087

510(k) Number K082087 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 23, 2008
Decision Date September 11, 2008
Days to Decision 50 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 116d · This submission: 50d
Pathway characteristics
Predicate-based equivalence.

IMD Device Classification - Class 1, General Controls

Product Code IMD Pack, Hot Or Cold, Disposable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5710
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 - IMD Pack, Hot Or Cold, Disposable

All 54
Devices cleared under the same product code (IMD) and FDA review panel - the closest regulatory comparables to K082087.
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NEO NEST
K112547 · Denovo Proucts, LLC · Mar 2012
BENGAY (R) HEAT THERAPY, PAIN RELIEVING PATCHES/PADS (VARIOUS)
K071710 · Johnson & Johnson Consumer Products, Inc. · Aug 2007
EYEFEEL OPHTHALMIC WARMER
K021843 · Bio-Lipid, Inc. · Sep 2002
ALLEGIANCE PORTA-WARM MATTRESS
K982652 · Allegiance Healthcare Corp. · Jan 1999
K082087 · EYEFEEL OPHTHALMIC WARMER
Download PDF FDA Summary Bio-Lipid, Inc.