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FDA 510(k)

FLUID DRAINAGE WICK

K-Number: K885232 · 1989-02-08

ApplicantVisitec Co.
Decision Date1989-02-08
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FLUID DRAINAGE WICK is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1989-02-08 under 510(k) number K885232. The device is classified under product code HOZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID DRAINAGE WICK?

FLUID DRAINAGE WICK is a medical device that received FDA 510(k) clearance on 1989-02-08. The listed applicant is Visitec Co.. The 510(k) number is K885232.

When did FLUID DRAINAGE WICK receive FDA 510(k) clearance?

FLUID DRAINAGE WICK received FDA 510(k) clearance on 1989-02-08, under 510(k) number K885232.

Who is the listed applicant for FLUID DRAINAGE WICK?

The FDA 510(k) record lists Visitec Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUID DRAINAGE WICK?

The FDA product code for FLUID DRAINAGE WICK is HOZ.

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Other records listing Visitec Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K953394VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}K945114VISITEC SCLERAL PLUGK945738VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEK945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSK942234VISITEC PRECISE-POINTK934269FIBEROPTIC ILLUMINATED INSTRUMENTS

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Related Devices (Code: HOZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K132796SUNTOUCH EYE SPEARHuizhou Foryou Medical Devices Co., Ltd.K130117NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDSNetwork Medical Products, Ltd.K091240ALPHAMED SURGICAL SPEAR, MODEL 70-5000Alphamed, Inc.K082460CENEFOM PVA SURGICAL SPEARLongtek Scientific Co., Ltd.K012196ULTRACELL ABSORBENT STICKUltracell Medical Technologies, Inc.K011191MEROCEL CORNELL LID AND LASH GUARD, MEROCEL AND KEROCEL OPHTHALMIC SPONGESMedtronic Xomed, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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