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FDA 510(k)

PRO-OPHTA STICKS

K-Number: K802794 · 1980-12-22

ApplicantSecol Co.
Decision Date1980-12-22
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PRO-OPHTA STICKS is the device name listed in this FDA 510(k) record. The listed applicant is Secol Co.. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K802794. 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 PRO-OPHTA STICKS?

PRO-OPHTA STICKS is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Secol Co.. The 510(k) number is K802794.

When did PRO-OPHTA STICKS receive FDA 510(k) clearance?

PRO-OPHTA STICKS received FDA 510(k) clearance on 1980-12-22, under 510(k) number K802794.

Who is the listed applicant for PRO-OPHTA STICKS?

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

What is the FDA product code for PRO-OPHTA STICKS?

The FDA product code for PRO-OPHTA STICKS is HOZ.

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Other records listing Secol 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.

K802790SOLVALINEK810111CELLONA PLASTER VARNISHK810109METAL SPLINTSK810110COBBLER'S CHIP SPLINTSK802793LOMATUELL OINTMENT DRESSINGK802791ZINC PASTE BANDAGE

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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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