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FDA 510(k)

ALCON FLUID INJECTOR

K-Number: K882723 · 1988-11-08

ApplicantAlcon Laboratories
Decision Date1988-11-08
Product CodeDQF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ALCON FLUID INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1988-11-08 under 510(k) number K882723. The device is classified under product code DQF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCON FLUID INJECTOR?

ALCON FLUID INJECTOR is a medical device that received FDA 510(k) clearance on 1988-11-08. The listed applicant is Alcon Laboratories. The 510(k) number is K882723.

When did ALCON FLUID INJECTOR receive FDA 510(k) clearance?

ALCON FLUID INJECTOR received FDA 510(k) clearance on 1988-11-08, under 510(k) number K882723.

Who is the listed applicant for ALCON FLUID INJECTOR?

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 FLUID INJECTOR?

The FDA product code for ALCON FLUID INJECTOR is DQF.

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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: DQF)

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.

K920177VERSA-VIALBioteque America, Inc.K880740MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGESpectramed, 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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