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FDA 510(k)

EYE PROCEDURE PACK

K-Number: K850340 · 1985-05-22

ApplicantMarwood Medical, Inc.
Decision Date1985-05-22
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EYE PROCEDURE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Marwood Medical, Inc.. It received FDA 510(k) clearance on 1985-05-22 under 510(k) number K850340. 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 EYE PROCEDURE PACK?

EYE PROCEDURE PACK is a medical device that received FDA 510(k) clearance on 1985-05-22. The listed applicant is Marwood Medical, Inc.. The 510(k) number is K850340.

When did EYE PROCEDURE PACK receive FDA 510(k) clearance?

EYE PROCEDURE PACK received FDA 510(k) clearance on 1985-05-22, under 510(k) number K850340.

Who is the listed applicant for EYE PROCEDURE PACK?

The FDA 510(k) record lists Marwood Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EYE PROCEDURE PACK?

The FDA product code for EYE PROCEDURE PACK is HOZ.

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Other records listing Marwood Medical, Inc. 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.

K850338EMERGENCY ROOM PACKK850339SPECIAL PROCEDURES PACKK850337CARDIAC CATHETERIZATION PACKK850341CARDIOVASCULAR SET UPK840620TPN/CVP DRESSING CHANGE KITK840619I.V. START KIT

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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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