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FDA 510(k)

EYE PAD

K-Number: K904896 · 1990-12-05

ApplicantUlti-Med Intl., Inc.
Decision Date1990-12-05
Product CodeHMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EYE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Ulti-Med Intl., Inc.. It received FDA 510(k) clearance on 1990-12-05 under 510(k) number K904896. The device is classified under product code HMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EYE PAD?

EYE PAD is a medical device that received FDA 510(k) clearance on 1990-12-05. The listed applicant is Ulti-Med Intl., Inc.. The 510(k) number is K904896.

When did EYE PAD receive FDA 510(k) clearance?

EYE PAD received FDA 510(k) clearance on 1990-12-05, under 510(k) number K904896.

Who is the listed applicant for EYE PAD?

The FDA 510(k) record lists Ulti-Med Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EYE PAD?

The FDA product code for EYE PAD is HMP.

Other records listing Ulti-Med Intl., 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.

K103011ULTICARE SAFETY INSULIN SYRINGEK923176SURGICAL INSTRUMENT KIT, DISPOSABLEK923175SURGICAL INSTRUMENT KIT, DISPOSABLEK920989SURGICAL INSTRUMENT KIT, DISPOSABLEK922828ULCER WOUND TRAYK914244STERILE CUSTOM SURGICAL KITS

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Related Devices (Code: HMP)

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.

K940333EYE PADCertified Safety Mfg., Inc.K921349STERILE,DISPOSABLE EYE DRESSINGDeroyal Industries, Inc.K883822FIRST AID KIT, EYE DRESSING NSN6545-00-853-6309Consolidated Industries of Greater Syracuse, Inc.K874411DONALDSON NATURAL EYEPATCH 'PATIENT PAK'Keeler Instruments, Inc.K864810LIDSPLINTPrecision Therapeutics, Inc.K861456SHEETS LYOPHILIZED COLLAGEN HEYEDRATORPantheon Products, 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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