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FDA 510(k)

EYE PADS

K-Number: K802799 · 1980-12-17

ApplicantSecol Co.
Decision Date1980-12-17
Product CodeHMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EYE PADS is the device name listed in this FDA 510(k) record. The listed applicant is Secol Co.. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802799. 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 PADS?

EYE PADS is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Secol Co.. The 510(k) number is K802799.

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

EYE PADS received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802799.

Who is the listed applicant for EYE PADS?

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 EYE PADS?

The FDA product code for EYE PADS is HMP.

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 SPLINTSK802794PRO-OPHTA STICKSK802793LOMATUELL OINTMENT DRESSING

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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.K904896EYE PADUlti-Med Intl., 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.

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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