Cleared Traditional

K840471 - EYE SPEAR

K840471 is an FDA 510(k) clearance for EYE SPEAR, manufactured by Surgicot, Inc.. The device is a Class 2 Ophthalmic device with product code HOZ cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K840471 · Surgicot, Inc. · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1984
Decision
42d
Days
Class 2
Risk

K840471 is an FDA 510(k) clearance for the EYE SPEAR. Classified as Sponge, Ophthalmic (product code HOZ), Class II - Special Controls.

Submitted by Surgicot, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 16, 1984 after a review of 42 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 Surgicot, Inc. devices

FDA 510(k) Submission Details - K840471

510(k) Number K840471 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 1984
Decision Date March 16, 1984
Days to Decision 42 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
68d faster than avg
Panel avg: 110d · This submission: 42d
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 24
Devices cleared under the same product code (HOZ) and FDA review panel - the closest regulatory comparables to K840471.
SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11
K850883 · Storz Instrument Co. · Mar 1985
OPERAID SURGICAL DRAIN
K841721 · Jedmed Instrument Co. · Nov 1984
EYE SPONGE OR SPEAR
K834356 · Jedmed Instrument Co. · Mar 1984
FLORET OPHTHALMIC EYE SPEAR
K830262 · Ritmed, Inc. · Apr 1983
PRO-OPHTA STICKS
K802794 · Secol Co. · Dec 1980