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FDA 510(k)

VISITEC MICRO-SPONGE SPEARS

K-Number: K896705 · 1990-01-11

ApplicantVisitec Co.
Decision Date1990-01-11
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISITEC MICRO-SPONGE SPEARS is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K896705. 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 VISITEC MICRO-SPONGE SPEARS?

VISITEC MICRO-SPONGE SPEARS is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Visitec Co.. The 510(k) number is K896705.

When did VISITEC MICRO-SPONGE SPEARS receive FDA 510(k) clearance?

VISITEC MICRO-SPONGE SPEARS received FDA 510(k) clearance on 1990-01-11, under 510(k) number K896705.

Who is the listed applicant for VISITEC MICRO-SPONGE SPEARS?

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 VISITEC MICRO-SPONGE SPEARS?

The FDA product code for VISITEC MICRO-SPONGE SPEARS 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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