FDA 510(k)

CELLULOSE EYE STICK

K-Number: K761155 · 1976-12-16

Decision Date1976-12-16

Product CodeHOZ

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

CELLULOSE EYE STICK is the device name listed in this FDA 510(k) record. The listed applicant is Winn Hirsch & Assoc.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761155. 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 CELLULOSE EYE STICK?

CELLULOSE EYE STICK is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Winn Hirsch & Assoc.. The 510(k) number is K761155.

When did CELLULOSE EYE STICK receive FDA 510(k) clearance?

CELLULOSE EYE STICK received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761155.

Who is the listed applicant for CELLULOSE EYE STICK?

The FDA 510(k) record lists Winn Hirsch & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CELLULOSE EYE STICK?

The FDA product code for CELLULOSE EYE STICK is HOZ.

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Other records listing Winn Hirsch & Assoc. as applicant

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Related Devices (Code: HOZ)

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.