Atlas FDA

VISI-SPEAR EYE SPONGE

FDA 510(k) clearance K933872 · decided 1993-12-27

Clearance details

K-number
K933872
Device name
VISI-SPEAR EYE SPONGE
Applicant
Visitec Co.
Decision
Substantially Equivalent
Date received
1993-08-06
Decision date
1993-12-27
Days to decision
143 days
Clearance type
Traditional
Product code
HOZ
Device class
2
Regulation number
886.4790
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Sarasota, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
SUNTOUCH EYE SPEAR (K132796)Huizhou Foryou Medical Devices Co., Ltd.2013-10-30
NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDS (K130117)Network Medical Products, Ltd.2013-10-29
ALPHAMED SURGICAL SPEAR, MODEL 70-5000 (K091240)Alphamed, Inc.2009-10-23
CENEFOM PVA SURGICAL SPEAR (K082460)Longtek Scientific Co., Ltd.2008-12-15
ULTRACELL ABSORBENT STICK (K012196)Ultracell Medical Technologies, Inc.2001-08-24
MEROCEL CORNELL LID AND LASH GUARD, MEROCEL AND KEROCEL OPHTHALMIC SPONGES (K011191)Medtronic Xomed, Inc.2001-06-26
PRESCOTT'S SURGICAL SPEAR (K003842)Prescott'S, Inc.2001-04-13
ML EYE SPEAR, MODEL ML 27 ES (K002279)Med-Logics, Inc.2000-08-18
M-PACT CORNEAL LIGHT SHIELD (K993883)M-Pact Corp.1999-12-21
DRAINAGE WICK; SURGICAL SPEARS AND SPONGES, CORNEAL LIGHT SHIELD, INSTRUMENT WIPE (K990671)Hurricane Medical1999-05-10
SOF-SUCTION FLUID EVACUATION SYSTEM (K990749)X-Tech Medical, LLC1999-04-02
THE FREMSTAD RING (K982599)Ophthalmic Solutions, LLC1999-02-16

Recalls involving this device

No recalls on record reference this clearance.