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FDA 510(k)

AMPCO OPTHALMIC TRAY

K-Number: K842983 · 1985-05-22

ApplicantAssociated Medical Products Co.
Decision Date1985-05-22
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AMPCO OPTHALMIC TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Associated Medical Products Co.. It received FDA 510(k) clearance on 1985-05-22 under 510(k) number K842983. 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 AMPCO OPTHALMIC TRAY?

AMPCO OPTHALMIC TRAY is a medical device that received FDA 510(k) clearance on 1985-05-22. The listed applicant is Associated Medical Products Co.. The 510(k) number is K842983.

When did AMPCO OPTHALMIC TRAY receive FDA 510(k) clearance?

AMPCO OPTHALMIC TRAY received FDA 510(k) clearance on 1985-05-22, under 510(k) number K842983.

Who is the listed applicant for AMPCO OPTHALMIC TRAY?

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

What is the FDA product code for AMPCO OPTHALMIC TRAY?

The FDA product code for AMPCO OPTHALMIC TRAY is HOZ.

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Other records listing Associated Medical Products Co. as applicant

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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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