Cleared Traditional

K850883 - SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11

K850883 is an FDA 510(k) clearance for SCLERAL SPONGE II, manufactured by Storz Instrument Co.. The device is a Class 2 Ophthalmic device with product code HOZ cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K850883 · Storz Instrument Co. · Ophthalmic device
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Mar 1985
Decision
16d
Days
Class 2
Risk

K850883 is an FDA 510(k) clearance for the SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11. Classified as Sponge, Ophthalmic (product code HOZ), Class II - Special Controls.

Submitted by Storz Instrument Co. (St. Louis, US). The FDA issued a Cleared decision on March 20, 1985 after a review of 16 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4790 - the FDA ophthalmic 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 Storz Instrument Co. devices

FDA 510(k) Submission Details - K850883

510(k) Number K850883 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 04, 1985
Decision Date March 20, 1985
Days to Decision 16 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 110d · This submission: 16d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HOZ Device Classification - Class 2, Special Controls

Product Code HOZ Sponge, Ophthalmic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.4790
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 Ophthalmic devices follow this clearance model.

Regulatory Peers - HOZ Sponge, Ophthalmic

All 34
Devices cleared under the same product code (HOZ) and FDA review panel - the closest regulatory comparables to K850883.
AMPCO OPTHALMIC TRAY
K842983 · Associated Medical Products Co. · May 1985
STERILE EYE SURGERY KITS
K842990 · Biological & Environmental Control Laboratories · May 1985
PMS OPHTHALMOLOGY PACK-PMS EYE TRAY/PACK
K850050 · Professional Medical Services · Apr 1985
OPERAID SURGICAL DRAIN
K841721 · Jedmed Instrument Co. · Nov 1984
EYE SPONGE OR SPEAR
K834356 · Jedmed Instrument Co. · Mar 1984
EYE SPEAR
K840471 · Surgicot, Inc. · Mar 1984