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FDA 510(k)

ALCON SITE(R)-COMPATIBLE CASSETTE

K-Number: K881682 · 1988-07-01

ApplicantAlcon Laboratories
Decision Date1988-07-01
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALCON SITE(R)-COMPATIBLE CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1988-07-01 under 510(k) number K881682. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCON SITE(R)-COMPATIBLE CASSETTE?

ALCON SITE(R)-COMPATIBLE CASSETTE is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is Alcon Laboratories. The 510(k) number is K881682.

When did ALCON SITE(R)-COMPATIBLE CASSETTE receive FDA 510(k) clearance?

ALCON SITE(R)-COMPATIBLE CASSETTE received FDA 510(k) clearance on 1988-07-01, under 510(k) number K881682.

Who is the listed applicant for ALCON SITE(R)-COMPATIBLE CASSETTE?

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

What is the FDA product code for ALCON SITE(R)-COMPATIBLE CASSETTE?

The FDA product code for ALCON SITE(R)-COMPATIBLE CASSETTE is KYG.

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Other records listing Alcon Laboratories 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.

K062624NEXT GENERATION LASERK062865SMALL VOLUME SYRINGEK000148RGP MULTI-PURPOSE SOLUTION ID 100136K984573OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROPK990480OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVERK984575MULTI-PURPOSE DISINFECTING SOLUTION ID 90746

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Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, 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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